Canonical Allele Identifier: CA1882579756
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255883G= , CM000671.2:g.133255883G= GRCh38
NC_000009.11:g.136131270G= , CM000671.1:g.136131270G= GRCh37
NC_000009.10:g.135121091G= NCBI36
NG_006669.1:g.21785C=
NG_006669.2:g.24333C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.877C=
ENST00000647353.1:n.54-4731C=
ENST00000679909.1:c.28+19279C= ENSP00000506089.1:n.28+19279C=
ENST00000453660.3:n.859C=
ENST00000538324.2:c.845C= ENSP00000483018.1:p.Ala282=
ENST00000611156.4:c.845C= ENSP00000483265.1:p.Ala282=
NM_020469.2:c.848C= NP_065202.2:p.Ala283=
NM_020469.3:c.848C= NP_065202.2:p.Ala283=