Canonical Allele Identifier: CA671793614
Gene: PTS HGNC NCBI

Linked Data

dbSNP Id: rs1453307199
MyVariant Identifiers: chr11:g.112097125G>C (hg19) chr11:g.112226402G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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