Canonical Allele Identifier: CA467782867
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131578G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256191G>C , CM000671.2:g.133256191G>C GRCh38
NC_000009.11:g.136131578G>C , CM000671.1:g.136131578G>C GRCh37
NC_000009.10:g.135121399G>C NCBI36
NG_006669.1:g.21477C>G
NG_006669.2:g.24025C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.569C>G
ENST00000647353.1:n.54-5039C>G
ENST00000651471.1:n.495C>G
ENST00000679909.1:c.28+18971C>G ENSP00000506089.1:n.28+18971C>G
ENST00000453660.3:n.551C>G
ENST00000538324.2:c.537C>G ENSP00000483018.1:p.Arg179=
ENST00000611156.4:c.537C>G ENSP00000483265.1:p.Arg179=
NM_020469.2:c.540C>G NP_065202.2:p.Arg180=
NM_020469.3:c.540C>G NP_065202.2:p.Arg180=