Canonical Allele Identifier: CA466186154
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829162467
gnomAD v3: 9-97700133-G-C
gnomAD v4: 9-97700133-G-C
MyVariant Identifiers: chr9:g.100462415G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700133G>C , CM000671.2:g.97700133G>C GRCh38
NC_000009.11:g.100462415G>C , CM000671.1:g.100462415G>C GRCh37
NC_000009.10:g.99502236G>C NCBI36
NG_011642.1:g.2277C>G , LRG_471:g.2277C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.689G>C (KRT18P13)
NR_147055.1:n.1501-62C>G (PTCSC2)