Canonical Allele Identifier: CA467783442
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136132798C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257411C>T , CM000671.2:g.133257411C>T GRCh38
NC_000009.11:g.136132798C>T , CM000671.1:g.136132798C>T GRCh37
NC_000009.10:g.135122619C>T NCBI36
NG_006669.1:g.20257G>A
NG_006669.2:g.22805G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.401G>A
ENST00000647353.1:n.54-6259G>A
ENST00000651471.1:n.329+631G>A
ENST00000679909.1:c.28+17751G>A ENSP00000506089.1:n.28+17751G>A
ENST00000453660.3:n.383G>A
ENST00000538324.2:c.369G>A ENSP00000483018.1:p.Lys123=
ENST00000611156.4:c.369G>A ENSP00000483265.1:p.Lys123=
NM_020469.2:c.372G>A NP_065202.2:p.Lys124=
NM_020469.3:c.372G>A NP_065202.2:p.Lys124=