Canonical Allele Identifier: CA375686772
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257525A>T , CM000671.2:g.133257525A>T GRCh38
NC_000009.11:g.136132912A>T , CM000671.1:g.136132912A>T GRCh37
NC_000009.10:g.135122733A>T NCBI36
NG_006669.1:g.20142T>A
NG_006669.2:g.22690T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.287T>A
ENST00000647353.1:n.54-6373T>A
ENST00000651471.1:n.329+517T>A
ENST00000679909.1:c.28+17637T>A ENSP00000506089.1:n.28+17637T>A
ENST00000453660.3:n.269T>A
ENST00000538324.2:c.257T>A ENSP00000483018.1:p.Val86Glu
ENST00000611156.4:c.257T>A ENSP00000483265.1:p.Val86Glu
NM_020469.2:c.257T>A NP_065202.2:p.Val86Glu
NM_020469.3:c.257T>A NP_065202.2:p.Val86Glu