Canonical Allele Identifier: CA467780826
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs373302536
MyVariant Identifiers: chr9:g.136130837T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255450T>C , CM000671.2:g.133255450T>C GRCh38
NC_000009.11:g.136130837T>C , CM000671.1:g.136130837T>C GRCh37
NC_000009.10:g.135120658T>C NCBI36
NG_006669.1:g.22218A>G
NG_006669.2:g.24766A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1310A>G
ENST00000647353.1:n.54-4298A>G
ENST00000679909.1:c.28+19712A>G ENSP00000506089.1:n.28+19712A>G
ENST00000453660.3:n.1292A>G
ENST00000611156.4:c.*216A>G ENSP00000483265.1:n.*216A>G
NM_020469.2:c.*216A>G NP_065202.2:n.*216A>G
NM_020469.3:c.*216A>G NP_065202.2:n.*216A>G