Canonical Allele Identifier: CA1866667993
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830601662

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852503T>C , CM000671.2:g.97852503T>C GRCh38
NC_000009.11:g.100614785T>C , CM000671.1:g.100614785T>C GRCh37
NC_000009.10:g.99654606T>C NCBI36
NG_011979.1:g.4249T>C

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+373A>G
XR_930159.1:n.218+373A>G
XR_930160.1:n.218+373A>G
XR_930161.1:n.218+373A>G
NR_147055.1:n.165+413A>G