Canonical Allele Identifier: CA653191702

Gene: PTCSC2

Linked Data

• COSMIC: COSN20524263

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851727C>T , CM000671.2:g.97851727C>T	GRCh38
NC_000009.11:g.100614009C>T , CM000671.1:g.100614009C>T	GRCh37
NC_000009.10:g.99653830C>T	NCBI36
NG_011979.1:g.3473C>T

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+1149G>A
XR_930159.1:n.218+1149G>A
XR_930160.1:n.218+1149G>A
XR_930161.1:n.218+1149G>A
NR_147055.1:n.165+1189G>A