Canonical Allele Identifier: CA375683387

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131091C>A (hg19) ; chr9:g.133255704C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255704C>A , CM000671.2:g.133255704C>A	GRCh38
NC_000009.11:g.136131091C>A , CM000671.1:g.136131091C>A	GRCh37
NC_000009.10:g.135120912C>A	NCBI36
NG_006669.1:g.21964G>T
NG_006669.2:g.24512G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1056G>T
ENST00000647353.1:n.54-4552G>T
ENST00000679909.1:c.28+19458G>T	ENSP00000506089.1:n.28+19458G>T
ENST00000453660.3:n.1038G>T
ENST00000538324.2:c.1024G>T	ENSP00000483018.1:p.Ala342Ser
ENST00000611156.4:c.1024G>T	ENSP00000483265.1:p.Ala342Ser
NM_020469.2:c.1027G>T	NP_065202.2:p.Ala343Ser
NM_020469.3:c.1027G>T	NP_065202.2:p.Ala343Ser