Canonical Allele Identifier: CA467783509
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136132813A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257426A>C , CM000671.2:g.133257426A>C GRCh38
NC_000009.11:g.136132813A>C , CM000671.1:g.136132813A>C GRCh37
NC_000009.10:g.135122634A>C NCBI36
NG_006669.1:g.20242T>G
NG_006669.2:g.22790T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.386T>G
ENST00000647353.1:n.54-6274T>G
ENST00000651471.1:n.329+616T>G
ENST00000679909.1:c.28+17736T>G ENSP00000506089.1:n.28+17736T>G
ENST00000453660.3:n.368T>G
ENST00000538324.2:c.354T>G ENSP00000483018.1:p.Thr118=
ENST00000611156.4:c.354T>G ENSP00000483265.1:p.Thr118=
NM_020469.2:c.357T>G NP_065202.2:p.Thr119=
NM_020469.3:c.357T>G NP_065202.2:p.Thr119=