Canonical Allele Identifier: CA5305652

Gene: ABO

Linked Data

• dbSNP Id: rs7466899
• ExAC: 9:136131069 G / A
• gnomAD v2: 9-136131069-G-A
• gnomAD v3: 9-133255682-G-A
• gnomAD v4: 9-133255682-G-A
• MyVariant Identifiers: chr9:g.136131069G>A (hg19) ; chr9:g.133255682G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255682G>A , CM000671.2:g.133255682G>A	GRCh38
NC_000009.11:g.136131069G>A , CM000671.1:g.136131069G>A	GRCh37
NC_000009.10:g.135120890G>A	NCBI36
NG_006669.1:g.21986C>T
NG_006669.2:g.24534C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1078C>T
ENST00000647353.1:n.54-4530C>T
ENST00000679909.1:c.28+19480C>T	ENSP00000506089.1:n.28+19480C>T
ENST00000453660.3:n.1060C>T
ENST00000538324.2:c.1046C>T	ENSP00000483018.1:p.Ala349Val
ENST00000611156.4:c.1046C>T	ENSP00000483265.1:p.Ala349Val
NM_020469.2:c.1049C>T	NP_065202.2:p.Ala350Val
NM_020469.3:c.1049C>T	NP_065202.2:p.Ala350Val