Canonical Allele Identifier: CA869018917
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712819
MyVariant Identifiers: chr9:g.100614225_100614226insCG (hg19) chr9:g.97851943_97851944insCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851944_97851945insGC , CM000671.2:g.97851944_97851945insGC GRCh38
NC_000009.11:g.100614226_100614227insGC , CM000671.1:g.100614226_100614227insGC GRCh37
NC_000009.10:g.99654047_99654048insGC NCBI36
NG_011979.1:g.3690_3691insGC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+932_218+933insCG
XR_930159.1:n.218+932_218+933insCG
XR_930160.1:n.218+932_218+933insCG
XR_930161.1:n.218+932_218+933insCG
NR_147055.1:n.165+972_165+973insCG
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