Canonical Allele Identifier: CA467780027
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130701G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255314G>T , CM000671.2:g.133255314G>T GRCh38
NC_000009.11:g.136130701G>T , CM000671.1:g.136130701G>T GRCh37
NC_000009.10:g.135120522G>T NCBI36
NG_006669.1:g.22354C>A
NG_006669.2:g.24902C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1446C>A
ENST00000647353.1:n.54-4162C>A
ENST00000679909.1:c.28+19848C>A ENSP00000506089.1:n.28+19848C>A
ENST00000453660.3:n.1428C>A
ENST00000611156.4:c.*352C>A ENSP00000483265.1:n.*352C>A
NM_020469.2:c.*352C>A NP_065202.2:n.*352C>A
NM_020469.3:c.*352C>A NP_065202.2:n.*352C>A
Search 100 bp 5'
Search 100 bp 3'