Canonical Allele Identifier: CA2720199614

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1830592361

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851935_97851936insGGGGGGGGGGGGGGGG , CM000671.2:g.97851935_97851936insGGGGGGGGGGGGGGGG	GRCh38
NC_000009.11:g.100614217_100614218insGGGGGGGGGGGGGGGG , CM000671.1:g.100614217_100614218insGGGGGGGGGGGGGGGG	GRCh37
NC_000009.10:g.99654038_99654039insGGGGGGGGGGGGGGGG	NCBI36
NG_011979.1:g.3681_3682insGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+942_218+943insCCCCCCCCCCCCCCCC
XR_930159.1:n.218+942_218+943insCCCCCCCCCCCCCCCC
XR_930160.1:n.218+942_218+943insCCCCCCCCCCCCCCCC
XR_930161.1:n.218+942_218+943insCCCCCCCCCCCCCCCC
NR_147055.1:n.165+982_165+983insCCCCCCCCCCCCCCCC