Canonical Allele Identifier: CA197053098

Gene: PTCSC2

Linked Data

• dbSNP Id: rs906580114
• gnomAD v3: 9-97793929-G-T
• gnomAD v4: 9-97793929-G-T
• MyVariant Identifiers: chr9:g.100556211G>T (hg19) ; chr9:g.97793929G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97793929G>T , CM000671.2:g.97793929G>T	GRCh38
NC_000009.11:g.100556211G>T , CM000671.1:g.100556211G>T	GRCh37
NC_000009.10:g.99596032G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930161.1:n.363+15966C>A
NR_147055.1:n.777+10322C>A