Canonical Allele Identifier: CA1866667876

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1830600245

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97852417A>T , CM000671.2:g.97852417A>T	GRCh38
NC_000009.11:g.100614699A>T , CM000671.1:g.100614699A>T	GRCh37
NC_000009.10:g.99654520A>T	NCBI36
NG_011979.1:g.4163A>T

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+459T>A
XR_930159.1:n.218+459T>A
XR_930160.1:n.218+459T>A
XR_930161.1:n.218+459T>A
NR_147055.1:n.165+499T>A