Canonical Allele Identifier: CA467781431

Gene: ABO

Linked Data

• dbSNP Id: rs1044735139
• gnomAD v4: 9-133255532-G-C
• MyVariant Identifiers: chr9:g.136130919G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255532G>C , CM000671.2:g.133255532G>C	GRCh38
NC_000009.11:g.136130919G>C , CM000671.1:g.136130919G>C	GRCh37
NC_000009.10:g.135120740G>C	NCBI36
NG_006669.1:g.22136C>G
NG_006669.2:g.24684C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1228C>G
ENST00000647353.1:n.54-4380C>G
ENST00000679909.1:c.28+19630C>G	ENSP00000506089.1:n.28+19630C>G
ENST00000453660.3:n.1210C>G
ENST00000611156.4:c.*134C>G	ENSP00000483265.1:n.*134C>G
NM_020469.2:c.*134C>G	NP_065202.2:n.*134C>G
NM_020469.3:c.*134C>G	NP_065202.2:n.*134C>G