Canonical Allele Identifier: CA686396098
Gene: SLCO1B3 HGNC NCBI
SLCO1B3-SLCO1B7 HGNC NCBI

Linked Data

dbSNP Id: rs1345723055
gnomAD v3: 12-20864733-CCT-C
gnomAD v4: 12-20864733-CCT-C
MyVariant Identifiers: chr12:g.21017668_21017669del (hg19) chr12:g.20864734_20864735del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20864734_20864735del , CM000674.2:g.20864734_20864735del GRCh38
NC_000012.11:g.21017668_21017669del , CM000674.1:g.21017668_21017669del GRCh37
NC_000012.10:g.20908935_20908936del NCBI36
NG_032071.1:g.59031_59032del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381545.8:c.727+1880_727+1881del (SLCO1B3) MANE Select ENSP00000370956.4:n.727+1880_727+1881del
ENST00000261196.6:c.727+1880_727+1881del (SLCO1B3) ENSP00000261196.2:n.727+1880_727+1881del
ENST00000381541.7:c.359+6163_359+6164del (SLCO1B3-SLCO1B7) ENSP00000370952.3:n.359+6163_359+6164del
ENST00000381545.7:c.727+1880_727+1881del (SLCO1B3) ENSP00000370956.3:n.727+1880_727+1881del
ENST00000540229.1:c.727+1880_727+1881del (SLCO1B3-SLCO1B7) ENSP00000441269.1:n.727+1880_727+1881del
ENST00000540853.5:c.727+1880_727+1881del (SLCO1B3) ENSP00000442000.1:n.727+1880_727+1881del
ENST00000544370.1:c.199+1880_199+1881del (SLCO1B3) ENSP00000443225.1:n.199+1880_199+1881del
NM_019844.3:c.727+1880_727+1881del (SLCO1B3) NP_062818.1:n.727+1880_727+1881del
NM_001349920.1:c.643+1880_643+1881del (SLCO1B3) NP_001336849.1:n.643+1880_643+1881del
NM_001349920.2:c.643+1880_643+1881del (SLCO1B3) NP_001336849.1:n.643+1880_643+1881del
NM_001371097.1:c.727+1880_727+1881del (SLCO1B3-SLCO1B7) NP_001358026.1:n.727+1880_727+1881del
NM_019844.4:c.727+1880_727+1881del (SLCO1B3) MANE Select NP_062818.1:n.727+1880_727+1881del
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