Canonical Allele Identifier: CA2516831436
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852077T>C , CM000671.2:g.97852077T>C GRCh38
NC_000009.11:g.100614359T>C , CM000671.1:g.100614359T>C GRCh37
NC_000009.10:g.99654180T>C NCBI36
NG_011979.1:g.3823T>C

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+799A>G
XR_930159.1:n.218+799A>G
XR_930160.1:n.218+799A>G
XR_930161.1:n.218+799A>G
NR_147055.1:n.165+839A>G