Canonical Allele Identifier: CA1127207959

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1587807016
• gnomAD v3: 9-97851893-A-C
• gnomAD v4: 9-97851893-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851893A>C , CM000671.2:g.97851893A>C	GRCh38
NC_000009.11:g.100614175A>C , CM000671.1:g.100614175A>C	GRCh37
NC_000009.10:g.99653996A>C	NCBI36
NG_011979.1:g.3639A>C

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+983T>G
XR_930159.1:n.218+983T>G
XR_930160.1:n.218+983T>G
XR_930161.1:n.218+983T>G
NR_147055.1:n.165+1023T>G