Canonical Allele Identifier: CA1866666584
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830586281
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851621G>A , CM000671.2:g.97851621G>A GRCh38
NC_000009.11:g.100613903G>A , CM000671.1:g.100613903G>A GRCh37
NC_000009.10:g.99653724G>A NCBI36
NG_011979.1:g.3367G>A

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+1255C>T
XR_930159.1:n.218+1255C>T
XR_930160.1:n.218+1255C>T
XR_930161.1:n.218+1255C>T
NR_147055.1:n.165+1295C>T
Search 100 bp 5'
Search 100 bp 3'