Canonical Allele Identifier: CA1882579064
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255611A= , CM000671.2:g.133255611A= GRCh38
NC_000009.11:g.136130998A= , CM000671.1:g.136130998A= GRCh37
NC_000009.10:g.135120819A= NCBI36
NG_006669.1:g.22057T=
NG_006669.2:g.24605T=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1149T=
ENST00000647353.1:n.54-4459T=
ENST00000679909.1:c.28+19551T= ENSP00000506089.1:n.28+19551T=
ENST00000453660.3:n.1131T=
ENST00000538324.2:c.1113T= ENSP00000483018.1:p.Pro371=
ENST00000611156.4:c.*55T= ENSP00000483265.1:n.*55T=
NM_020469.2:c.*55T= NP_065202.2:n.*55T=
NM_020469.3:c.*55T= NP_065202.2:n.*55T=