Canonical Allele Identifier: CA2615998867
Gene: PTS HGNC NCBI

Linked Data

gnomAD v4: 11-112226402-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226402G>A , CM000673.2:g.112226402G>A GRCh38
NC_000011.9:g.112097125G>A , CM000673.1:g.112097125G>A GRCh37
NC_000011.8:g.111602335G>A NCBI36
NG_008743.1:g.5038G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.7:c.-42G>A ENSP00000280362.3:n.-42G>A
ENST00000525645.1:n.34G>A
ENST00000528679.5:c.-42G>A ENSP00000435895.1:n.-42G>A
ENST00000531673.5:c.-42G>A ENSP00000433469.1:n.-42G>A
NM_000317.2:c.-42G>A NP_000308.1:n.-42G>A
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