Canonical Allele Identifier: CA860754270

Gene: ABO

Linked Data

• dbSNP Id: rs1231865182
• gnomAD v3: 9-133257213-C-T
• gnomAD v4: 9-133257213-C-T
• MyVariant Identifiers: chr9:g.136132600C>T (hg19) ; chr9:g.133257213C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257213C>T , CM000671.2:g.133257213C>T	GRCh38
NC_000009.11:g.136132600C>T , CM000671.1:g.136132600C>T	GRCh37
NC_000009.10:g.135122421C>T	NCBI36
NG_006669.1:g.20455G>A
NG_006669.2:g.23003G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.403+196G>A
ENST00000647353.1:n.54-6061G>A
ENST00000651471.1:n.329+829G>A
ENST00000679909.1:c.28+17949G>A	ENSP00000506089.1:n.28+17949G>A
ENST00000453660.3:n.385+196G>A
ENST00000538324.2:c.371+196G>A	ENSP00000483018.1:n.371+196G>A
ENST00000611156.4:c.371+196G>A	ENSP00000483265.1:n.371+196G>A
NM_020469.2:c.374+196G>A	NP_065202.2:n.374+196G>A
NM_020469.3:c.374+196G>A	NP_065202.2:n.374+196G>A