Canonical Allele Identifier: CA1127208584
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1209020520
gnomAD v3: 9-97851948-C-A
gnomAD v4: 9-97851948-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851948C>A , CM000671.2:g.97851948C>A GRCh38
NC_000009.11:g.100614230C>A , CM000671.1:g.100614230C>A GRCh37
NC_000009.10:g.99654051C>A NCBI36
NG_011979.1:g.3694C>A

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+928G>T
XR_930159.1:n.218+928G>T
XR_930160.1:n.218+928G>T
XR_930161.1:n.218+928G>T
NR_147055.1:n.165+968G>T