Canonical Allele Identifier: CA869019181

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1339195996
• MyVariant Identifiers: chr9:g.100614261G>C (hg19) ; chr9:g.97851979G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851979G>C , CM000671.2:g.97851979G>C	GRCh38
NC_000009.11:g.100614261G>C , CM000671.1:g.100614261G>C	GRCh37
NC_000009.10:g.99654082G>C	NCBI36
NG_011979.1:g.3725G>C

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+897C>G
XR_930159.1:n.218+897C>G
XR_930160.1:n.218+897C>G
XR_930161.1:n.218+897C>G
NR_147055.1:n.165+937C>G