Canonical Allele Identifier: CA1593535485
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156073982G= , CM000667.2:g.156073982G= GRCh38
NC_000005.9:g.155500992G= , CM000667.1:g.155500992G= GRCh37
NC_000005.8:g.155433570G= NCBI36
NG_008693.2:g.208639G= , LRG_205:g.208639G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-281-43896G= ENSP00000429378.1:n.-281-43896G=
XM_017009723.2:c.-207-49874G= XP_016865212.1:n.-207-49874G=
XM_017009724.1:c.-207-49874G= XP_016865213.1:n.-207-49874G=