Canonical Allele Identifier: CA1866668319
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1047014821

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852747G>C , CM000671.2:g.97852747G>C GRCh38
NC_000009.11:g.100615029G>C , CM000671.1:g.100615029G>C GRCh37
NC_000009.10:g.99654850G>C NCBI36
NG_011979.1:g.4493G>C

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+129C>G
XR_930159.1:n.218+129C>G
XR_930160.1:n.218+129C>G
XR_930161.1:n.218+129C>G
NR_147055.1:n.165+169C>G