Canonical Allele Identifier: CA200766407
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs4962040
MyVariant Identifiers: chr9:g.133258141G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258141G>A , CM000671.2:g.133258141G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-9C>T
ENST00000647353.1:n.54-6989C>T
ENST00000651471.1:n.239-9C>T
ENST00000679909.1:c.28+17021C>T ENSP00000506089.1:n.28+17021C>T
ENST00000453660.3:n.216-9C>T
ENST00000538324.2:c.204-9C>T ENSP00000483018.1:n.204-9C>T
ENST00000611156.4:c.204-9C>T ENSP00000483265.1:n.204-9C>T
NM_020469.2:c.204-9C>T NP_065202.2:n.204-9C>T
NM_020469.3:c.204-9C>T NP_065202.2:n.204-9C>T