Canonical Allele Identifier: CA1866666865

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1432871380

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851935G>T , CM000671.2:g.97851935G>T	GRCh38
NC_000009.11:g.100614217G>T , CM000671.1:g.100614217G>T	GRCh37
NC_000009.10:g.99654038G>T	NCBI36
NG_011979.1:g.3681G>T

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+941C>A
XR_930159.1:n.218+941C>A
XR_930160.1:n.218+941C>A
XR_930161.1:n.218+941C>A
NR_147055.1:n.165+981C>A