Canonical Allele Identifier: CA467780756
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130827G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255440G>A , CM000671.2:g.133255440G>A GRCh38
NC_000009.11:g.136130827G>A , CM000671.1:g.136130827G>A GRCh37
NC_000009.10:g.135120648G>A NCBI36
NG_006669.1:g.22228C>T
NG_006669.2:g.24776C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1320C>T
ENST00000647353.1:n.54-4288C>T
ENST00000679909.1:c.28+19722C>T ENSP00000506089.1:n.28+19722C>T
ENST00000453660.3:n.1302C>T
ENST00000611156.4:c.*226C>T ENSP00000483265.1:n.*226C>T
NM_020469.2:c.*226C>T NP_065202.2:n.*226C>T
NM_020469.3:c.*226C>T NP_065202.2:n.*226C>T
Search 100 bp 5'
Search 100 bp 3'