Canonical Allele Identifier: CA860763730
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1334944554
MyVariant Identifiers: chr9:g.133274216C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274216C>T , CM000671.2:g.133274216C>T GRCh38
NC_000009.11:g.136149632C>T , CM000671.1:g.136149632C>T GRCh37
NC_000009.10:g.135139453C>T NCBI36
NG_006669.1:g.3419G>A
NG_006669.2:g.5999G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+946G>A
ENST00000647353.1:n.53+946G>A
ENST00000651471.1:n.63+1746G>A
ENST00000679909.1:c.28+946G>A ENSP00000506089.1:n.28+946G>A
ENST00000453660.3:n.40+946G>A
ENST00000538324.2:c.28+946G>A ENSP00000483018.1:n.28+946G>A
ENST00000611156.4:c.28+946G>A ENSP00000483265.1:n.28+946G>A
NM_020469.2:c.28+946G>A NP_065202.2:n.28+946G>A
NM_020469.3:c.28+946G>A NP_065202.2:n.28+946G>A