Canonical Allele Identifier: CA869002484
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1406129410
gnomAD v3: 9-97786665-G-C
gnomAD v4: 9-97786665-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786665G>C , CM000671.2:g.97786665G>C GRCh38
NC_000009.11:g.100548947G>C , CM000671.1:g.100548947G>C GRCh37
NC_000009.10:g.99588768G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23230C>G
NR_147055.1:n.777+17586C>G