Canonical Allele Identifier: CA375686770
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.287T>G
ENST00000647353.1:n.54-6373T>G
ENST00000651471.1:n.329+517T>G
ENST00000679909.1:c.28+17637T>G ENSP00000506089.1:n.28+17637T>G
ENST00000453660.3:n.269T>G
ENST00000538324.2:c.257T>G ENSP00000483018.1:p.Val86Gly
ENST00000611156.4:c.257T>G ENSP00000483265.1:p.Val86Gly
NM_020469.2:c.257T>G NP_065202.2:p.Val86Gly
NM_020469.3:c.257T>G NP_065202.2:p.Val86Gly