Canonical Allele Identifier: CA869019013
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1308604953

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851947_97851948insTC , CM000671.2:g.97851947_97851948insTC GRCh38
NC_000009.11:g.100614229_100614230insTC , CM000671.1:g.100614229_100614230insTC GRCh37
NC_000009.10:g.99654050_99654051insTC NCBI36
NG_011979.1:g.3693_3694insTC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+929_218+930insAG
XR_930159.1:n.218+929_218+930insAG
XR_930160.1:n.218+929_218+930insAG
XR_930161.1:n.218+929_218+930insAG
NR_147055.1:n.165+969_165+970insAG