Canonical Allele Identifier: CA1127208057

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1587807047
• gnomAD v3: 9-97851926-A-C
• gnomAD v4: 9-97851926-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851926A>C , CM000671.2:g.97851926A>C	GRCh38
NC_000009.11:g.100614208A>C , CM000671.1:g.100614208A>C	GRCh37
NC_000009.10:g.99654029A>C	NCBI36
NG_011979.1:g.3672A>C

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+950T>G
XR_930159.1:n.218+950T>G
XR_930160.1:n.218+950T>G
XR_930161.1:n.218+950T>G
NR_147055.1:n.165+990T>G