Canonical Allele Identifier: CA1882580337
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256099T= , CM000671.2:g.133256099T= GRCh38
NC_000009.11:g.136131486T= , CM000671.1:g.136131486T= GRCh37
NC_000009.10:g.135121307T= NCBI36
NG_006669.1:g.21569A=
NG_006669.2:g.24117A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.661A=
ENST00000647353.1:n.54-4947A=
ENST00000679909.1:c.28+19063A= ENSP00000506089.1:n.28+19063A=
ENST00000453660.3:n.643A=
ENST00000538324.2:c.629A= ENSP00000483018.1:p.Asp210=
ENST00000611156.4:c.629A= ENSP00000483265.1:p.Asp210=
NM_020469.2:c.632A= NP_065202.2:p.Asp211=
NM_020469.3:c.632A= NP_065202.2:p.Asp211=