Canonical Allele Identifier: CA1866666894
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830592929

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851939_97851943dup , CM000671.2:g.97851939_97851943dup GRCh38
NC_000009.11:g.100614221_100614225dup , CM000671.1:g.100614221_100614225dup GRCh37
NC_000009.10:g.99654042_99654046dup NCBI36
NG_011979.1:g.3685_3689dup

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+936_218+940dup
XR_930159.1:n.218+936_218+940dup
XR_930160.1:n.218+936_218+940dup
XR_930161.1:n.218+936_218+940dup
NR_147055.1:n.165+976_165+980dup