Canonical Allele Identifier: CA197059076
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs969597568

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852069T>C , CM000671.2:g.97852069T>C GRCh38
NC_000009.11:g.100614351T>C , CM000671.1:g.100614351T>C GRCh37
NC_000009.10:g.99654172T>C NCBI36
NG_011979.1:g.3815T>C

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+807A>G
XR_930159.1:n.218+807A>G
XR_930160.1:n.218+807A>G
XR_930161.1:n.218+807A>G
NR_147055.1:n.165+847A>G