Canonical Allele Identifier: CA467780935
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130852T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255465T>C , CM000671.2:g.133255465T>C GRCh38
NC_000009.11:g.136130852T>C , CM000671.1:g.136130852T>C GRCh37
NC_000009.10:g.135120673T>C NCBI36
NG_006669.1:g.22203A>G
NG_006669.2:g.24751A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1295A>G
ENST00000647353.1:n.54-4313A>G
ENST00000679909.1:c.28+19697A>G ENSP00000506089.1:n.28+19697A>G
ENST00000453660.3:n.1277A>G
ENST00000611156.4:c.*201A>G ENSP00000483265.1:n.*201A>G
NM_020469.2:c.*201A>G NP_065202.2:n.*201A>G
NM_020469.3:c.*201A>G NP_065202.2:n.*201A>G