Canonical Allele Identifier: CA2692330738

Gene: ABO

Linked Data

• gnomAD v4: 9-133257985-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257985G>T , CM000671.2:g.133257985G>T	GRCh38
NC_000009.11:g.136133372G>T , CM000671.1:g.136133372G>T	GRCh37
NC_000009.10:g.135123193G>T	NCBI36
NG_006669.1:g.19682C>A
NG_006669.2:g.22230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+112C>A
ENST00000647353.1:n.54-6833C>A
ENST00000651471.1:n.329+57C>A
ENST00000679909.1:c.28+17177C>A	ENSP00000506089.1:n.28+17177C>A
ENST00000453660.3:n.251+112C>A
ENST00000538324.2:c.239+112C>A	ENSP00000483018.1:n.239+112C>A
ENST00000611156.4:c.239+112C>A	ENSP00000483265.1:n.239+112C>A
NM_020469.2:c.239+112C>A	NP_065202.2:n.239+112C>A
NM_020469.3:c.239+112C>A	NP_065202.2:n.239+112C>A