Canonical Allele Identifier: CA1866666808
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851927_97851928delinsCA , CM000671.2:g.97851927_97851928delinsCA GRCh38
NC_000009.11:g.100614209_100614210delinsCA , CM000671.1:g.100614209_100614210delinsCA GRCh37
NC_000009.10:g.99654030_99654031delinsCA NCBI36
NG_011979.1:g.3673_3674delinsCA

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+948_218+949delinsTG
XR_930159.1:n.218+948_218+949delinsTG
XR_930160.1:n.218+948_218+949delinsTG
XR_930161.1:n.218+948_218+949delinsTG
NR_147055.1:n.165+988_165+989delinsTG