Canonical Allele Identifier: CA467781346
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130910T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255523T>A , CM000671.2:g.133255523T>A GRCh38
NC_000009.11:g.136130910T>A , CM000671.1:g.136130910T>A GRCh37
NC_000009.10:g.135120731T>A NCBI36
NG_006669.1:g.22145A>T
NG_006669.2:g.24693A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1237A>T
ENST00000647353.1:n.54-4371A>T
ENST00000679909.1:c.28+19639A>T ENSP00000506089.1:n.28+19639A>T
ENST00000453660.3:n.1219A>T
ENST00000611156.4:c.*143A>T ENSP00000483265.1:n.*143A>T
NM_020469.2:c.*143A>T NP_065202.2:n.*143A>T
NM_020469.3:c.*143A>T NP_065202.2:n.*143A>T