Canonical Allele Identifier: CA1866667376
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830596301

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852070A>T , CM000671.2:g.97852070A>T GRCh38
NC_000009.11:g.100614352A>T , CM000671.1:g.100614352A>T GRCh37
NC_000009.10:g.99654173A>T NCBI36
NG_011979.1:g.3816A>T

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+806T>A
XR_930159.1:n.218+806T>A
XR_930160.1:n.218+806T>A
XR_930161.1:n.218+806T>A
NR_147055.1:n.165+846T>A