Canonical Allele Identifier: CA2692330683

Gene: ABO

Linked Data

• gnomAD v4: 9-133257679-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257679C>A , CM000671.2:g.133257679C>A	GRCh38
NC_000009.11:g.136133066C>A , CM000671.1:g.136133066C>A	GRCh37
NC_000009.10:g.135122887C>A	NCBI36
NG_006669.1:g.19988G>T
NG_006669.2:g.22536G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.270-137G>T
ENST00000647353.1:n.54-6527G>T
ENST00000651471.1:n.329+363G>T
ENST00000679909.1:c.28+17483G>T	ENSP00000506089.1:n.28+17483G>T
ENST00000453660.3:n.252-137G>T
ENST00000538324.2:c.240-137G>T	ENSP00000483018.1:n.240-137G>T
ENST00000611156.4:c.240-137G>T	ENSP00000483265.1:n.240-137G>T
NM_020469.2:c.240-137G>T	NP_065202.2:n.240-137G>T
NM_020469.3:c.240-137G>T	NP_065202.2:n.240-137G>T