Canonical Allele Identifier: CA228595064
Gene: PTS HGNC NCBI

Linked Data

dbSNP Id: rs971334186

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226403G>A , CM000673.2:g.112226403G>A GRCh38
NC_000011.9:g.112097126G>A , CM000673.1:g.112097126G>A GRCh37
NC_000011.8:g.111602336G>A NCBI36
NG_008743.1:g.5039G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.7:c.-41G>A ENSP00000280362.3:n.-41G>A
ENST00000525645.1:n.35G>A
ENST00000528679.5:c.-41G>A ENSP00000435895.1:n.-41G>A
ENST00000531673.5:c.-41G>A ENSP00000433469.1:n.-41G>A
NM_000317.2:c.-41G>A NP_000308.1:n.-41G>A