Canonical Allele Identifier: CA869004610

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1370027677
• MyVariant Identifiers: chr9:g.100556122_100556124del (hg19) ; chr9:g.97793840_97793842del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97793844_97793846del , CM000671.2:g.97793844_97793846del	GRCh38
NC_000009.11:g.100556126_100556128del , CM000671.1:g.100556126_100556128del	GRCh37
NC_000009.10:g.99595947_99595949del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930161.1:n.363+16053_363+16055del
XR_930162.1:n.6529_6531del
NR_147055.1:n.777+10409_777+10411del