Canonical Allele Identifier: CA1882580315
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256091T= , CM000671.2:g.133256091T= GRCh38
NC_000009.11:g.136131478T= , CM000671.1:g.136131478T= GRCh37
NC_000009.10:g.135121299T= NCBI36
NG_006669.1:g.21577A=
NG_006669.2:g.24125A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.669A=
ENST00000647353.1:n.54-4939A=
ENST00000679909.1:c.28+19071A= ENSP00000506089.1:n.28+19071A=
ENST00000453660.3:n.651A=
ENST00000538324.2:c.637A= ENSP00000483018.1:p.Met213=
ENST00000611156.4:c.637A= ENSP00000483265.1:p.Met213=
NM_020469.2:c.640A= NP_065202.2:p.Met214=
NM_020469.3:c.640A= NP_065202.2:p.Met214=