Canonical Allele Identifier: CA1866667114
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712832

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851949_97851950insTC , CM000671.2:g.97851949_97851950insTC GRCh38
NC_000009.11:g.100614231_100614232insTC , CM000671.1:g.100614231_100614232insTC GRCh37
NC_000009.10:g.99654052_99654053insTC NCBI36
NG_011979.1:g.3695_3696insTC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+927_218+928insAG
XR_930159.1:n.218+927_218+928insAG
XR_930160.1:n.218+927_218+928insAG
XR_930161.1:n.218+927_218+928insAG
NR_147055.1:n.165+967_165+968insAG