Canonical Allele Identifier: CA1866668431
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852906G= , CM000671.2:g.97852906G= GRCh38
NC_000009.11:g.100615188G= , CM000671.1:g.100615188G= GRCh37
NC_000009.10:g.99655009G= NCBI36
NG_011979.1:g.4652G=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.188C=
XR_930159.1:n.188C=
XR_930160.1:n.188C=
XR_930161.1:n.188C=
NR_147055.1:n.165+10C=