Canonical Allele Identifier: CA467780627
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130807C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255420C>A , CM000671.2:g.133255420C>A GRCh38
NC_000009.11:g.136130807C>A , CM000671.1:g.136130807C>A GRCh37
NC_000009.10:g.135120628C>A NCBI36
NG_006669.1:g.22248G>T
NG_006669.2:g.24796G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1340G>T
ENST00000647353.1:n.54-4268G>T
ENST00000679909.1:c.28+19742G>T ENSP00000506089.1:n.28+19742G>T
ENST00000453660.3:n.1322G>T
ENST00000611156.4:c.*246G>T ENSP00000483265.1:n.*246G>T
NM_020469.2:c.*246G>T NP_065202.2:n.*246G>T
NM_020469.3:c.*246G>T NP_065202.2:n.*246G>T