Canonical Allele Identifier: CA2692330614

Gene: ABO

Linked Data

• gnomAD v4: 9-133257618-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257618C>A , CM000671.2:g.133257618C>A	GRCh38
NC_000009.11:g.136133005C>A , CM000671.1:g.136133005C>A	GRCh37
NC_000009.10:g.135122826C>A	NCBI36
NG_006669.1:g.20049G>T
NG_006669.2:g.22597G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.270-76G>T
ENST00000647353.1:n.54-6466G>T
ENST00000651471.1:n.329+424G>T
ENST00000679909.1:c.28+17544G>T	ENSP00000506089.1:n.28+17544G>T
ENST00000453660.3:n.252-76G>T
ENST00000538324.2:c.240-76G>T	ENSP00000483018.1:n.240-76G>T
ENST00000611156.4:c.240-76G>T	ENSP00000483265.1:n.240-76G>T
NM_020469.2:c.240-76G>T	NP_065202.2:n.240-76G>T
NM_020469.3:c.240-76G>T	NP_065202.2:n.240-76G>T