Canonical Allele Identifier: CA1866690963
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1587788540

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793811A>G , CM000671.2:g.97793811A>G GRCh38
NC_000009.11:g.100556093A>G , CM000671.1:g.100556093A>G GRCh37
NC_000009.10:g.99595914A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16084T>C
XR_930162.1:n.6496A>G
NR_147055.1:n.777+10440T>C