Canonical Allele Identifier: CA467781384
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130914T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255527T>A , CM000671.2:g.133255527T>A GRCh38
NC_000009.11:g.136130914T>A , CM000671.1:g.136130914T>A GRCh37
NC_000009.10:g.135120735T>A NCBI36
NG_006669.1:g.22141A>T
NG_006669.2:g.24689A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1233A>T
ENST00000647353.1:n.54-4375A>T
ENST00000679909.1:c.28+19635A>T ENSP00000506089.1:n.28+19635A>T
ENST00000453660.3:n.1215A>T
ENST00000611156.4:c.*139A>T ENSP00000483265.1:n.*139A>T
NM_020469.2:c.*139A>T NP_065202.2:n.*139A>T
NM_020469.3:c.*139A>T NP_065202.2:n.*139A>T