Canonical Allele Identifier: CA467781061
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130870T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255483T>G , CM000671.2:g.133255483T>G GRCh38
NC_000009.11:g.136130870T>G , CM000671.1:g.136130870T>G GRCh37
NC_000009.10:g.135120691T>G NCBI36
NG_006669.1:g.22185A>C
NG_006669.2:g.24733A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1277A>C
ENST00000647353.1:n.54-4331A>C
ENST00000679909.1:c.28+19679A>C ENSP00000506089.1:n.28+19679A>C
ENST00000453660.3:n.1259A>C
ENST00000611156.4:c.*183A>C ENSP00000483265.1:n.*183A>C
NM_020469.2:c.*183A>C NP_065202.2:n.*183A>C
NM_020469.3:c.*183A>C NP_065202.2:n.*183A>C
Search 100 bp 5'
Search 100 bp 3'