Canonical Allele Identifier: CA1593483768
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967226T= , CM000667.2:g.155967226T= GRCh38
NC_000005.9:g.155394236T= , CM000667.1:g.155394236T= GRCh37
NC_000005.8:g.155326814T= NCBI36
NG_008693.2:g.101883T= , LRG_205:g.101883T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96802T= ENSP00000429378.1:n.-282+96802T=
XM_017009723.2:c.-208+96802T= XP_016865212.1:n.-208+96802T=
XM_017009724.1:c.-207-156630T= XP_016865213.1:n.-207-156630T=