Canonical Allele Identifier: CA2551319366
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852633T>C , CM000671.2:g.97852633T>C GRCh38
NC_000009.11:g.100614915T>C , CM000671.1:g.100614915T>C GRCh37
NC_000009.10:g.99654736T>C NCBI36
NG_011979.1:g.4379T>C

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+243A>G
XR_930159.1:n.218+243A>G
XR_930160.1:n.218+243A>G
XR_930161.1:n.218+243A>G
NR_147055.1:n.165+283A>G