Canonical Allele Identifier: CA2692330570

Gene: ABO

Linked Data

• gnomAD v4: 9-133257548-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257548C>G , CM000671.2:g.133257548C>G	GRCh38
NC_000009.11:g.136132935C>G , CM000671.1:g.136132935C>G	GRCh37
NC_000009.10:g.135122756C>G	NCBI36
NG_006669.1:g.20119G>C
NG_006669.2:g.22667G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.270-6G>C
ENST00000647353.1:n.54-6396G>C
ENST00000651471.1:n.329+494G>C
ENST00000679909.1:c.28+17614G>C	ENSP00000506089.1:n.28+17614G>C
ENST00000453660.3:n.252-6G>C
ENST00000538324.2:c.240-6G>C	ENSP00000483018.1:n.240-6G>C
ENST00000611156.4:c.240-6G>C	ENSP00000483265.1:n.240-6G>C
NM_020469.2:c.240-6G>C	NP_065202.2:n.240-6G>C
NM_020469.3:c.240-6G>C	NP_065202.2:n.240-6G>C