Canonical Allele Identifier: CA466186147
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.100462413C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700131C>G , CM000671.2:g.97700131C>G GRCh38
NC_000009.11:g.100462413C>G , CM000671.1:g.100462413C>G GRCh37
NC_000009.10:g.99502234C>G NCBI36
NG_011642.1:g.2279G>C , LRG_471:g.2279G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.687C>G (KRT18P13)
NR_147055.1:n.1501-60G>C (PTCSC2)