Canonical Allele Identifier: CA466186187
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.100462421G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700139G>C , CM000671.2:g.97700139G>C GRCh38
NC_000009.11:g.100462421G>C , CM000671.1:g.100462421G>C GRCh37
NC_000009.10:g.99502242G>C NCBI36
NG_011642.1:g.2271C>G , LRG_471:g.2271C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.695G>C (KRT18P13)
NR_147055.1:n.1501-68C>G (PTCSC2)