Canonical Allele Identifier: CA467853039
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131269G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255882G>A , CM000671.2:g.133255882G>A GRCh38
NC_000009.11:g.136131269G>A , CM000671.1:g.136131269G>A GRCh37
NC_000009.10:g.135121090G>A NCBI36
NG_006669.1:g.21786C>T
NG_006669.2:g.24334C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.878C>T
ENST00000647353.1:n.54-4730C>T
ENST00000679909.1:c.28+19280C>T ENSP00000506089.1:n.28+19280C>T
ENST00000453660.3:n.860C>T
ENST00000538324.2:c.846C>T ENSP00000483018.1:p.Ala282=
ENST00000611156.4:c.846C>T ENSP00000483265.1:p.Ala282=
NM_020469.2:c.849C>T NP_065202.2:p.Ala283=
NM_020469.3:c.849C>T NP_065202.2:p.Ala283=