Canonical Allele Identifier: CA11378874
Community Standard Title: NM_005630.3(SLCO2A1):c.1691-105C>T
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133936002G>A , CM000665.2:g.133936002G>A GRCh38
NC_000003.11:g.133654846G>A , CM000665.1:g.133654846G>A GRCh37
NC_000003.10:g.135137536G>A NCBI36
NG_031964.2:g.121183C>T
NG_031964.3:g.121183C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.1691-105C>T MANE Select NP_005621.2:n.1691-105C>T
ENST00000310926.11:c.1691-105C>T MANE Select ENSP00000311291.4:n.1691-105C>T
NM_005630.2:c.1691-105C>T NP_005621.2:n.1691-105C>T
ENST00000310926.8:c.1691-105C>T ENSP00000311291.4:n.1691-105C>T
ENST00000481359.3:c.*253-105C>T ENSP00000420028.3:n.*253-105C>T
ENST00000493729.5:c.1463-105C>T ENSP00000418893.1:n.1463-105C>T
XM_011513090.1:c.*251C>T XP_011511392.1:n.*251C>T
XM_017007077.1:c.1187-105C>T XP_016862566.1:n.1187-105C>T
XM_024453721.1:c.*251C>T XP_024309489.1:n.*251C>T