Canonical Allele Identifier: CA653192400
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786690C>A , CM000671.2:g.97786690C>A GRCh38
NC_000009.11:g.100548972C>A , CM000671.1:g.100548972C>A GRCh37
NC_000009.10:g.99588793C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23205G>T
XR_930162.1:n.25C>A
NR_147055.1:n.777+17561G>T