Canonical Allele Identifier: CA197059057

Gene: PTCSC2

Linked Data

• dbSNP Id: rs184690826
• MyVariant Identifiers: chr9:g.100614229C>T (hg19) ; chr9:g.97851947C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851947C>T , CM000671.2:g.97851947C>T	GRCh38
NC_000009.11:g.100614229C>T , CM000671.1:g.100614229C>T	GRCh37
NC_000009.10:g.99654050C>T	NCBI36
NG_011979.1:g.3693C>T

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+929G>A
XR_930159.1:n.218+929G>A
XR_930160.1:n.218+929G>A
XR_930161.1:n.218+929G>A
NR_147055.1:n.165+969G>A