Canonical Allele Identifier: CA375683393
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255704C>T , CM000671.2:g.133255704C>T GRCh38
NC_000009.11:g.136131091C>T , CM000671.1:g.136131091C>T GRCh37
NC_000009.10:g.135120912C>T NCBI36
NG_006669.1:g.21964G>A
NG_006669.2:g.24512G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1056G>A
ENST00000647353.1:n.54-4552G>A
ENST00000679909.1:c.28+19458G>A ENSP00000506089.1:n.28+19458G>A
ENST00000453660.3:n.1038G>A
ENST00000538324.2:c.1024G>A ENSP00000483018.1:p.Ala342Thr
ENST00000611156.4:c.1024G>A ENSP00000483265.1:p.Ala342Thr
NM_020469.2:c.1027G>A NP_065202.2:p.Ala343Thr
NM_020469.3:c.1027G>A NP_065202.2:p.Ala343Thr