Canonical Allele Identifier: CA2690903719
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700131del , CM000671.2:g.97700131del GRCh38
NC_000009.11:g.100462413del , CM000671.1:g.100462413del GRCh37
NC_000009.10:g.99502234del NCBI36
NG_011642.1:g.2280del , LRG_471:g.2280del

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.687del (KRT18P13)
NR_147055.1:n.1501-59del (PTCSC2)