Canonical Allele Identifier: CA1593483786
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967271G= , CM000667.2:g.155967271G= GRCh38
NC_000005.9:g.155394281G= , CM000667.1:g.155394281G= GRCh37
NC_000005.8:g.155326859G= NCBI36
NG_008693.2:g.101928G= , LRG_205:g.101928G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96847G= ENSP00000429378.1:n.-282+96847G=
XM_017009723.2:c.-208+96847G= XP_016865212.1:n.-208+96847G=
XM_017009724.1:c.-207-156585G= XP_016865213.1:n.-207-156585G=