Canonical Allele Identifier: CA1866594692
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700130C= , CM000671.2:g.97700130C= GRCh38
NC_000009.11:g.100462412C= , CM000671.1:g.100462412C= GRCh37
NC_000009.10:g.99502233C= NCBI36
NG_011642.1:g.2280G= , LRG_471:g.2280G=

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.686C= (KRT18P13)
NR_147055.1:n.1501-59G= (PTCSC2)