Canonical Allele Identifier: CA1882583089

Gene: ABO

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258116G>T , CM000671.2:g.133258116G>T	GRCh38
NG_006669.1:g.19548C>A
NG_006669.2:g.22099C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.250C>A
ENST00000647353.1:n.54-6964C>A
ENST00000651471.1:n.255C>A
ENST00000679909.1:c.28+17046C>A	ENSP00000506089.1:n.28+17046C>A
ENST00000453660.3:n.232C>A
ENST00000538324.2:c.220C>A	ENSP00000483018.1:p.Pro74Thr
ENST00000611156.4:c.220C>A	ENSP00000483265.1:p.Pro74Thr
NM_020469.2:c.220C>A	NP_065202.2:p.Pro74Thr
NM_020469.3:c.220C>A	NP_065202.2:p.Pro74Thr