Canonical Allele Identifier: CA197059077
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs981053479

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852090G>A , CM000671.2:g.97852090G>A GRCh38
NC_000009.11:g.100614372G>A , CM000671.1:g.100614372G>A GRCh37
NC_000009.10:g.99654193G>A NCBI36
NG_011979.1:g.3836G>A

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+786C>T
XR_930159.1:n.218+786C>T
XR_930160.1:n.218+786C>T
XR_930161.1:n.218+786C>T
NR_147055.1:n.165+826C>T