Canonical Allele Identifier: CA1127157834
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829980868
gnomAD v3: 9-97786681-T-C
gnomAD v4: 9-97786681-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786681T>C , CM000671.2:g.97786681T>C GRCh38
NC_000009.11:g.100548963T>C , CM000671.1:g.100548963T>C GRCh37
NC_000009.10:g.99588784T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23214A>G
XR_930162.1:n.16T>C
NR_147055.1:n.777+17570A>G