Canonical Allele Identifier: CA2690903720
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700140del , CM000671.2:g.97700140del GRCh38
NC_000009.11:g.100462422del , CM000671.1:g.100462422del GRCh37
NC_000009.10:g.99502243del NCBI36
NG_011642.1:g.2272del , LRG_471:g.2272del

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.696del (KRT18P13)
NR_147055.1:n.1501-67del (PTCSC2)