Canonical Allele Identifier: CA1866691025
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830045577

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793939A>G , CM000671.2:g.97793939A>G GRCh38
NC_000009.11:g.100556221A>G , CM000671.1:g.100556221A>G GRCh37
NC_000009.10:g.99596042A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+15956T>C
NR_147055.1:n.777+10312T>C