Canonical Allele Identifier: CA13721358
Gene: SLCO1A2 HGNC NCBI

Linked Data

dbSNP Id: rs4149000
gnomAD v2: 12-21447997-C-T
gnomAD v3: 12-21295063-C-T
gnomAD v4: 12-21295063-C-T
MyVariant Identifiers: chr12:g.21447997C>T (hg19) chr12:g.21295063C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21295063C>T , CM000674.2:g.21295063C>T GRCh38
NC_000012.11:g.21447997C>T , CM000674.1:g.21447997C>T GRCh37
NC_000012.10:g.21339264C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000683939.1:c.1271+534G>A MANE Select ENSP00000508235.1:n.1271+534G>A
ENST00000307378.10:c.1271+534G>A ENSP00000305974.6:n.1271+534G>A
ENST00000458504.5:c.875+534G>A ENSP00000394854.1:n.875+534G>A
ENST00000463718.5:n.1562+534G>A
ENST00000480394.5:n.1833G>A
ENST00000544020.5:c.*850+534G>A ENSP00000440154.1:n.*850+534G>A
ENST00000544290.5:c.*850+534G>A ENSP00000438348.1:n.*850+534G>A
NM_021094.3:c.1271+534G>A NP_066580.1:n.1271+534G>A
NM_134431.3:c.1271+534G>A NP_602307.1:n.1271+534G>A
XM_005253474.3:c.1271+534G>A XP_005253531.1:n.1271+534G>A
XM_005253477.2:c.1211+534G>A XP_005253534.1:n.1211+534G>A
XM_011520818.1:c.1271+534G>A XP_011519120.1:n.1271+534G>A
XM_011520819.1:c.1271+534G>A XP_011519121.1:n.1271+534G>A
XM_011520820.1:c.1265+534G>A XP_011519122.1:n.1265+534G>A
XM_011520821.1:c.347+534G>A XP_011519123.1:n.347+534G>A
XM_005253477.3:c.1211+534G>A XP_005253534.1:n.1211+534G>A
XM_011520820.3:c.1265+534G>A XP_011519122.1:n.1265+534G>A
XM_011520821.2:c.347+534G>A XP_011519123.1:n.347+534G>A
XM_017019849.1:c.1271+534G>A XP_016875338.1:n.1271+534G>A
XM_017019850.1:c.1211+534G>A XP_016875339.1:n.1211+534G>A
XM_024449138.1:c.1271+534G>A XP_024304906.1:n.1271+534G>A
XM_024449139.1:c.1271+534G>A XP_024304907.1:n.1271+534G>A
NM_021094.4:c.1271+534G>A NP_066580.1:n.1271+534G>A
NM_001386878.1:c.1271+534G>A NP_001373807.1:n.1271+534G>A
NM_001386879.1:c.1271+534G>A MANE Select NP_001373808.1:n.1271+534G>A
NM_001386880.1:c.1271+534G>A NP_001373809.1:n.1271+534G>A
NM_001386881.1:c.1271+534G>A NP_001373810.1:n.1271+534G>A
NM_001386882.1:c.1271+534G>A NP_001373811.1:n.1271+534G>A
NM_001386886.1:c.1265+534G>A NP_001373815.1:n.1265+534G>A
NM_001386887.1:c.1271+534G>A NP_001373816.1:n.1271+534G>A
NM_001386890.1:c.803+534G>A NP_001373819.1:n.803+534G>A
NM_001386908.1:c.1010+534G>A NP_001373837.1:n.1010+534G>A
NM_001386919.1:c.1010+534G>A NP_001373848.1:n.1010+534G>A
NM_001386920.1:c.803+534G>A NP_001373849.1:n.803+534G>A
NM_001386921.1:c.971+534G>A NP_001373850.1:n.971+534G>A
NM_001386922.1:c.875+534G>A NP_001373851.1:n.875+534G>A
NM_001386926.1:c.1265+534G>A NP_001373855.1:n.1265+534G>A
NM_001386927.1:c.1010+534G>A NP_001373856.1:n.1010+534G>A
NM_001386929.1:c.875+534G>A NP_001373858.1:n.875+534G>A
NM_001386931.1:c.803+534G>A NP_001373860.1:n.803+534G>A
NM_001386937.1:c.875+534G>A NP_001373866.1:n.875+534G>A
NM_001386938.1:c.875+534G>A NP_001373867.1:n.875+534G>A
NM_001386939.1:c.875+534G>A NP_001373868.1:n.875+534G>A
NM_001386940.1:c.875+534G>A NP_001373869.1:n.875+534G>A
NM_001386946.1:c.1211+534G>A NP_001373875.1:n.1211+534G>A
NM_001386947.1:c.1265+534G>A NP_001373876.1:n.1265+534G>A
NM_001386948.1:c.1211+534G>A NP_001373877.1:n.1211+534G>A
NM_001386949.1:c.1265+534G>A NP_001373878.1:n.1265+534G>A
NM_001386951.1:c.1211+534G>A NP_001373880.1:n.1211+534G>A
NM_001386952.1:c.1211+534G>A NP_001373881.1:n.1211+534G>A
NM_001386953.1:c.803+534G>A NP_001373882.1:n.803+534G>A
NM_001386954.1:c.803+534G>A NP_001373883.1:n.803+534G>A
NM_001386958.1:c.1211+534G>A NP_001373887.1:n.1211+534G>A
NM_001386959.1:c.1211+534G>A NP_001373888.1:n.1211+534G>A
NM_001386960.1:c.1265+534G>A NP_001373889.1:n.1265+534G>A
NM_001386961.1:c.803+534G>A NP_001373890.1:n.803+534G>A
NM_001386962.1:c.875+534G>A NP_001373891.1:n.875+534G>A
NM_001386963.1:c.1010+534G>A NP_001373892.1:n.1010+534G>A
NM_134431.5:c.1271+534G>A NP_602307.1:n.1271+534G>A
NR_170340.1:n.1377+534G>A
NR_170341.1:n.1270+534G>A
NR_170343.1:n.1911G>A
NM_001386882.2:c.1271+534G>A NP_001373811.1:n.1271+534G>A
Search 100 bp 5'
Search 100 bp 3'