Canonical Allele Identifier: CA375686752
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257515A>C , CM000671.2:g.133257515A>C GRCh38
NC_000009.11:g.136132902A>C , CM000671.1:g.136132902A>C GRCh37
NC_000009.10:g.135122723A>C NCBI36
NG_006669.1:g.20153T>G
NG_006669.2:g.22701T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.297T>G
ENST00000647353.1:n.54-6363T>G
ENST00000651471.1:n.329+527T>G
ENST00000679909.1:c.28+17647T>G ENSP00000506089.1:n.28+17647T>G
ENST00000453660.3:n.279T>G
ENST00000538324.2:c.265T>G ENSP00000483018.1:p.Trp89Gly
ENST00000611156.4:c.265T>G ENSP00000483265.1:p.Trp89Gly
NM_020469.2:c.268T>G NP_065202.2:p.Trp90Gly
NM_020469.3:c.268T>G NP_065202.2:p.Trp90Gly