Canonical Allele Identifier: CA2786163885

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274098G>T , CM000671.2:g.133274098G>T	GRCh38
NC_000009.11:g.136149514G>T , CM000671.1:g.136149514G>T	GRCh37
NC_000009.10:g.135139335G>T	NCBI36
NG_006669.1:g.3537C>A
NG_006669.2:g.6117C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.58+1064C>A
ENST00000647353.1:n.53+1064C>A
ENST00000651471.1:n.63+1864C>A
ENST00000679909.1:c.28+1064C>A	ENSP00000506089.1:n.28+1064C>A
ENST00000453660.3:n.40+1064C>A
ENST00000538324.2:c.28+1064C>A	ENSP00000483018.1:n.28+1064C>A
ENST00000611156.4:c.28+1064C>A	ENSP00000483265.1:n.28+1064C>A
NM_020469.2:c.28+1064C>A	NP_065202.2:n.28+1064C>A
NM_020469.3:c.28+1064C>A	NP_065202.2:n.28+1064C>A