Canonical Allele Identifier: CA467782954
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131674G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256287G>A , CM000671.2:g.133256287G>A GRCh38
NC_000009.11:g.136131674G>A , CM000671.1:g.136131674G>A GRCh37
NC_000009.10:g.135121495G>A NCBI36
NG_006669.1:g.21381C>T
NG_006669.2:g.23929C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.473C>T
ENST00000647353.1:n.54-5135C>T
ENST00000651471.1:n.399C>T
ENST00000679909.1:c.28+18875C>T ENSP00000506089.1:n.28+18875C>T
ENST00000453660.3:n.455C>T
ENST00000538324.2:c.441C>T ENSP00000483018.1:p.His147=
ENST00000611156.4:c.441C>T ENSP00000483265.1:p.His147=
NM_020469.2:c.444C>T NP_065202.2:p.His148=
NM_020469.3:c.444C>T NP_065202.2:p.His148=