Canonical Allele Identifier: CA354616759
Community Standard Title: NM_005630.3(SLCO2A1):c.1106-1G>C
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133947446C>G , CM000665.2:g.133947446C>G GRCh38
NC_000003.11:g.133666290C>G , CM000665.1:g.133666290C>G GRCh37
NC_000003.10:g.135148980C>G NCBI36
NG_031964.2:g.109739G>C
NG_031964.3:g.109739G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.1106-1G>C MANE Select NP_005621.2:n.1106-1G>C
ENST00000310926.11:c.1106-1G>C MANE Select ENSP00000311291.4:n.1106-1G>C
NM_005630.2:c.1106-1G>C NP_005621.2:n.1106-1G>C
ENST00000310926.8:c.1106-1G>C ENSP00000311291.4:n.1106-1G>C
ENST00000462770.5:n.686-1G>C
ENST00000481359.3:c.1105+1090G>C ENSP00000420028.3:n.1105+1090G>C
ENST00000493729.5:c.878-1G>C ENSP00000418893.1:n.878-1G>C
XM_011513090.1:c.1106-1G>C XP_011511392.1:n.1106-1G>C
XM_017007077.1:c.602-1G>C XP_016862566.1:n.602-1G>C
XM_024453721.1:c.1106-1G>C XP_024309489.1:n.1106-1G>C