Canonical Allele Identifier: CA1882579345
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255719T= , CM000671.2:g.133255719T= GRCh38
NC_000009.11:g.136131106T= , CM000671.1:g.136131106T= GRCh37
NC_000009.10:g.135120927T= NCBI36
NG_006669.1:g.21949A=
NG_006669.2:g.24497A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1041A=
ENST00000647353.1:n.54-4567A=
ENST00000679909.1:c.28+19443A= ENSP00000506089.1:n.28+19443A=
ENST00000453660.3:n.1023A=
ENST00000538324.2:c.1009A= ENSP00000483018.1:p.Lys337=
ENST00000611156.4:c.1009A= ENSP00000483265.1:p.Lys337=
NM_020469.2:c.1012A= NP_065202.2:p.Lys338=
NM_020469.3:c.1012A= NP_065202.2:p.Lys338=