Canonical Allele Identifier: CA1127157816
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829980478
gnomAD v3: 9-97786634-T-C
gnomAD v4: 9-97786634-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786634T>C , CM000671.2:g.97786634T>C GRCh38
NC_000009.11:g.100548916T>C , CM000671.1:g.100548916T>C GRCh37
NC_000009.10:g.99588737T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23261A>G
NR_147055.1:n.777+17617A>G