Canonical Allele Identifier: CA197059060
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs4743137
gnomAD v3: 9-97851950-C-A
gnomAD v4: 9-97851950-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851950C>A , CM000671.2:g.97851950C>A GRCh38
NC_000009.11:g.100614232C>A , CM000671.1:g.100614232C>A GRCh37
NC_000009.10:g.99654053C>A NCBI36
NG_011979.1:g.3696C>A

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+926G>T
XR_930159.1:n.218+926G>T
XR_930160.1:n.218+926G>T
XR_930161.1:n.218+926G>T
NR_147055.1:n.165+966G>T