Canonical Allele Identifier: CA1127208358
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs66806500

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851938_97851939insCCCCCCCCCCCCC , CM000671.2:g.97851938_97851939insCCCCCCCCCCCCC GRCh38
NC_000009.11:g.100614220_100614221insCCCCCCCCCCCCC , CM000671.1:g.100614220_100614221insCCCCCCCCCCCCC GRCh37
NC_000009.10:g.99654041_99654042insCCCCCCCCCCCCC NCBI36
NG_011979.1:g.3684_3685insCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+940_218+941insGGGGGGGGGGGGG
XR_930159.1:n.218+940_218+941insGGGGGGGGGGGGG
XR_930160.1:n.218+940_218+941insGGGGGGGGGGGGG
XR_930161.1:n.218+940_218+941insGGGGGGGGGGGGG
NR_147055.1:n.165+980_165+981insGGGGGGGGGGGGG