Canonical Allele Identifier: CA1866668378
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852853G= , CM000671.2:g.97852853G= GRCh38
NC_000009.11:g.100615135G= , CM000671.1:g.100615135G= GRCh37
NC_000009.10:g.99654956G= NCBI36
NG_011979.1:g.4599G=

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+23C=
XR_930159.1:n.218+23C=
XR_930160.1:n.218+23C=
XR_930161.1:n.218+23C=
NR_147055.1:n.165+63C=