Canonical Allele Identifier: CA1866667392
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830596462

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852087C>G , CM000671.2:g.97852087C>G GRCh38
NC_000009.11:g.100614369C>G , CM000671.1:g.100614369C>G GRCh37
NC_000009.10:g.99654190C>G NCBI36
NG_011979.1:g.3833C>G

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+789G>C
XR_930159.1:n.218+789G>C
XR_930160.1:n.218+789G>C
XR_930161.1:n.218+789G>C
NR_147055.1:n.165+829G>C