Canonical Allele Identifier: CA467781419
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130918G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255531G>A , CM000671.2:g.133255531G>A GRCh38
NC_000009.11:g.136130918G>A , CM000671.1:g.136130918G>A GRCh37
NC_000009.10:g.135120739G>A NCBI36
NG_006669.1:g.22137C>T
NG_006669.2:g.24685C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1229C>T
ENST00000647353.1:n.54-4379C>T
ENST00000679909.1:c.28+19631C>T ENSP00000506089.1:n.28+19631C>T
ENST00000453660.3:n.1211C>T
ENST00000611156.4:c.*135C>T ENSP00000483265.1:n.*135C>T
NM_020469.2:c.*135C>T NP_065202.2:n.*135C>T
NM_020469.3:c.*135C>T NP_065202.2:n.*135C>T