Canonical Allele Identifier: CA1866667787
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852375A= , CM000671.2:g.97852375A= GRCh38
NC_000009.11:g.100614657A= , CM000671.1:g.100614657A= GRCh37
NC_000009.10:g.99654478A= NCBI36
NG_011979.1:g.4121A=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+501T=
XR_930159.1:n.218+501T=
XR_930160.1:n.218+501T=
XR_930161.1:n.218+501T=
NR_147055.1:n.165+541T=