Canonical Allele Identifier: CA2000616480
Gene: PTS HGNC NCBI

Linked Data

dbSNP Id: rs1440594489

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226404G>A , CM000673.2:g.112226404G>A GRCh38
NC_000011.9:g.112097127G>A , CM000673.1:g.112097127G>A GRCh37
NC_000011.8:g.111602337G>A NCBI36
NG_008743.1:g.5040G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.7:c.-40G>A ENSP00000280362.3:n.-40G>A
ENST00000525645.1:n.36G>A
ENST00000528679.5:c.-40G>A ENSP00000435895.1:n.-40G>A
ENST00000531673.5:c.-40G>A ENSP00000433469.1:n.-40G>A
NM_000317.2:c.-40G>A NP_000308.1:n.-40G>A