Canonical Allele Identifier: CA1866667704
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852312A= , CM000671.2:g.97852312A= GRCh38
NC_000009.11:g.100614594A= , CM000671.1:g.100614594A= GRCh37
NC_000009.10:g.99654415A= NCBI36
NG_011979.1:g.4058A=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+564T=
XR_930159.1:n.218+564T=
XR_930160.1:n.218+564T=
XR_930161.1:n.218+564T=
NR_147055.1:n.165+604T=