Canonical Allele Identifier: CA1127207923

Gene: PTCSC2

Linked Data

• gnomAD v3: 9-97851866-A-C
• gnomAD v4: 9-97851866-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851866A>C , CM000671.2:g.97851866A>C	GRCh38
NC_000009.11:g.100614148A>C , CM000671.1:g.100614148A>C	GRCh37
NC_000009.10:g.99653969A>C	NCBI36
NG_011979.1:g.3612A>C

Transcript Alleles

HGVS	Amino-acid change
XR_930158.1:n.218+1010T>G
XR_930159.1:n.218+1010T>G
XR_930160.1:n.218+1010T>G
XR_930161.1:n.218+1010T>G
NR_147055.1:n.165+1050T>G