Canonical Allele Identifier: CA466186152
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.100462414A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700132A>T , CM000671.2:g.97700132A>T GRCh38
NC_000009.11:g.100462414A>T , CM000671.1:g.100462414A>T GRCh37
NC_000009.10:g.99502235A>T NCBI36
NG_011642.1:g.2278T>A , LRG_471:g.2278T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.688A>T (KRT18P13)
NR_147055.1:n.1501-61T>A (PTCSC2)
Search 100 bp 5'
Search 100 bp 3'