Canonical Allele Identifier: CA1866690910
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830042385
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793694G>A , CM000671.2:g.97793694G>A GRCh38
NC_000009.11:g.100555976G>A , CM000671.1:g.100555976G>A GRCh37
NC_000009.10:g.99595797G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16201C>T
XR_930162.1:n.6379G>A
NR_147055.1:n.777+10557C>T
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