Canonical Allele Identifier: CA466186133
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829162280
gnomAD v3: 9-97700128-T-A
gnomAD v4: 9-97700128-T-A
MyVariant Identifiers: chr9:g.100462410T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700128T>A , CM000671.2:g.97700128T>A GRCh38
NC_000009.11:g.100462410T>A , CM000671.1:g.100462410T>A GRCh37
NC_000009.10:g.99502231T>A NCBI36
NG_011642.1:g.2282A>T , LRG_471:g.2282A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.684T>A (KRT18P13)
NR_147055.1:n.1501-57A>T (PTCSC2)
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