Canonical Allele Identifier: CA1593483790
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967275T= , CM000667.2:g.155967275T= GRCh38
NC_000005.9:g.155394285T= , CM000667.1:g.155394285T= GRCh37
NC_000005.8:g.155326863T= NCBI36
NG_008693.2:g.101932T= , LRG_205:g.101932T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96851T= ENSP00000429378.1:n.-282+96851T=
XM_017009723.2:c.-208+96851T= XP_016865212.1:n.-208+96851T=
XM_017009724.1:c.-207-156581T= XP_016865213.1:n.-207-156581T=