Canonical Allele Identifier: CA869018909

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1296672161
• MyVariant Identifiers: chr9:g.100614224_100614225insA (hg19) ; chr9:g.97851942_97851943insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851942_97851943insA , CM000671.2:g.97851942_97851943insA	GRCh38
NC_000009.11:g.100614224_100614225insA , CM000671.1:g.100614224_100614225insA	GRCh37
NC_000009.10:g.99654045_99654046insA	NCBI36
NG_011979.1:g.3688_3689insA

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+933_218+934insT
XR_930159.1:n.218+933_218+934insT
XR_930160.1:n.218+933_218+934insT
XR_930161.1:n.218+933_218+934insT
NR_147055.1:n.165+973_165+974insT