Canonical Allele Identifier: CA2615998852
Gene: PTS HGNC NCBI

Linked Data

gnomAD v4: 11-112226400-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226400G>C , CM000673.2:g.112226400G>C GRCh38
NC_000011.9:g.112097123G>C , CM000673.1:g.112097123G>C GRCh37
NC_000011.8:g.111602333G>C NCBI36
NG_008743.1:g.5036G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.7:c.-44G>C ENSP00000280362.3:n.-44G>C
ENST00000525645.1:n.32G>C
ENST00000528679.5:c.-44G>C ENSP00000435895.1:n.-44G>C
ENST00000531673.5:c.-44G>C ENSP00000433469.1:n.-44G>C
NM_000317.2:c.-44G>C NP_000308.1:n.-44G>C
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