Canonical Allele Identifier: CA1882579619
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255828G= , CM000671.2:g.133255828G= GRCh38
NC_000009.11:g.136131215G= , CM000671.1:g.136131215G= GRCh37
NC_000009.10:g.135121036G= NCBI36
NG_006669.1:g.21840C=
NG_006669.2:g.24388C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.932C=
ENST00000647353.1:n.54-4676C=
ENST00000679909.1:c.28+19334C= ENSP00000506089.1:n.28+19334C=
ENST00000453660.3:n.914C=
ENST00000538324.2:c.900C= ENSP00000483018.1:p.His300=
ENST00000611156.4:c.900C= ENSP00000483265.1:p.His300=
NM_020469.2:c.903C= NP_065202.2:p.His301=
NM_020469.3:c.903C= NP_065202.2:p.His301=