Canonical Allele Identifier: CA1866687880
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829980776

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786669G>T , CM000671.2:g.97786669G>T GRCh38
NC_000009.11:g.100548951G>T , CM000671.1:g.100548951G>T GRCh37
NC_000009.10:g.99588772G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23226C>A
XR_930162.1:n.4G>T
NR_147055.1:n.777+17582C>A