Canonical Allele Identifier: CA467852724
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1588637218
MyVariant Identifiers: chr9:g.136131326G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255939G>A , CM000671.2:g.133255939G>A GRCh38
NC_000009.11:g.136131326G>A , CM000671.1:g.136131326G>A GRCh37
NC_000009.10:g.135121147G>A NCBI36
NG_006669.1:g.21729C>T
NG_006669.2:g.24277C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.821C>T
ENST00000647353.1:n.54-4787C>T
ENST00000679909.1:c.28+19223C>T ENSP00000506089.1:n.28+19223C>T
ENST00000453660.3:n.803C>T
ENST00000538324.2:c.789C>T ENSP00000483018.1:p.Tyr263=
ENST00000611156.4:c.789C>T ENSP00000483265.1:p.Tyr263=
NM_020469.2:c.792C>T NP_065202.2:p.Tyr264=
NM_020469.3:c.792C>T NP_065202.2:p.Tyr264=