Canonical Allele Identifier: CA869018919
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1384653767
MyVariant Identifiers: chr9:g.100614225_100614226insCCG (hg19) chr9:g.97851943_97851944insCCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851945_97851946insGCC , CM000671.2:g.97851945_97851946insGCC GRCh38
NC_000009.11:g.100614227_100614228insGCC , CM000671.1:g.100614227_100614228insGCC GRCh37
NC_000009.10:g.99654048_99654049insGCC NCBI36
NG_011979.1:g.3691_3692insGCC

Transcript Alleles

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