Canonical Allele Identifier: CA200768505

Gene: ABO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133263862A>T , CM000671.2:g.133263862A>T	GRCh38
NG_006669.2:g.16353T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.59-1694T>A
ENST00000647353.1:n.53+11300T>A
ENST00000651471.1:n.64-1694T>A
ENST00000679909.1:c.28+11300T>A	ENSP00000506089.1:n.28+11300T>A
ENST00000453660.3:n.41-1694T>A
ENST00000538324.2:c.29-1694T>A	ENSP00000483018.1:n.29-1694T>A
ENST00000611156.4:c.29-1694T>A	ENSP00000483265.1:n.29-1694T>A
NM_020469.2:c.29-1694T>A	NP_065202.2:n.29-1694T>A
NM_020469.3:c.29-1694T>A	NP_065202.2:n.29-1694T>A