Canonical Allele Identifier: CA15621244
Gene: PTCSC2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs965513

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793827A>G , CM000671.2:g.97793827A>G GRCh38
NC_000009.11:g.100556109A>G , CM000671.1:g.100556109A>G GRCh37
NC_000009.10:g.99595930A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+16068T>C
XR_930162.1:n.6512A>G
NR_147055.1:n.777+10424T>C