Canonical Allele Identifier: CA1866666932
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851938_97851939delinsCG , CM000671.2:g.97851938_97851939delinsCG GRCh38
NC_000009.11:g.100614220_100614221delinsCG , CM000671.1:g.100614220_100614221delinsCG GRCh37
NC_000009.10:g.99654041_99654042delinsCG NCBI36
NG_011979.1:g.3684_3685delinsCG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+937_218+938delinsCG
XR_930159.1:n.218+937_218+938delinsCG
XR_930160.1:n.218+937_218+938delinsCG
XR_930161.1:n.218+937_218+938delinsCG
NR_147055.1:n.165+977_165+978delinsCG