Canonical Allele Identifier: CA1866668327
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1587807546

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852761T>G , CM000671.2:g.97852761T>G GRCh38
NC_000009.11:g.100615043T>G , CM000671.1:g.100615043T>G GRCh37
NC_000009.10:g.99654864T>G NCBI36
NG_011979.1:g.4507T>G

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+115A>C
XR_930159.1:n.218+115A>C
XR_930160.1:n.218+115A>C
XR_930161.1:n.218+115A>C
NR_147055.1:n.165+155A>C