Canonical Allele Identifier: CA869019150
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs952851487
gnomAD v3: 9-97851951-C-CCG
gnomAD v4: 9-97851951-C-CCG
MyVariant Identifiers: chr9:g.100614233_100614234insCG (hg19) chr9:g.97851951_97851952insCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851951_97851952insCG , CM000671.2:g.97851951_97851952insCG GRCh38
NC_000009.11:g.100614233_100614234insCG , CM000671.1:g.100614233_100614234insCG GRCh37
NC_000009.10:g.99654054_99654055insCG NCBI36
NG_011979.1:g.3697_3698insCG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+924_218+925insCG
XR_930159.1:n.218+924_218+925insCG
XR_930160.1:n.218+924_218+925insCG
XR_930161.1:n.218+924_218+925insCG
NR_147055.1:n.165+964_165+965insCG
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