Canonical Allele Identifier: CA1127207903
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs534039490
gnomAD v3: 9-97851810-C-A
gnomAD v4: 9-97851810-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851810C>A , CM000671.2:g.97851810C>A GRCh38
NC_000009.11:g.100614092C>A , CM000671.1:g.100614092C>A GRCh37
NC_000009.10:g.99653913C>A NCBI36
NG_011979.1:g.3556C>A

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1066G>T
XR_930159.1:n.218+1066G>T
XR_930160.1:n.218+1066G>T
XR_930161.1:n.218+1066G>T
NR_147055.1:n.165+1106G>T