Canonical Allele Identifier: CA1882580326
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256096A= , CM000671.2:g.133256096A= GRCh38
NC_000009.11:g.136131483A= , CM000671.1:g.136131483A= GRCh37
NC_000009.10:g.135121304A= NCBI36
NG_006669.1:g.21572T=
NG_006669.2:g.24120T=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.664T=
ENST00000647353.1:n.54-4944T=
ENST00000679909.1:c.28+19066T= ENSP00000506089.1:n.28+19066T=
ENST00000453660.3:n.646T=
ENST00000538324.2:c.632T= ENSP00000483018.1:p.Val211=
ENST00000611156.4:c.632T= ENSP00000483265.1:p.Val211=
NM_020469.2:c.635T= NP_065202.2:p.Val212=
NM_020469.3:c.635T= NP_065202.2:p.Val212=