Canonical Allele Identifier: CA1593483767
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967223G= , CM000667.2:g.155967223G= GRCh38
NC_000005.9:g.155394233G= , CM000667.1:g.155394233G= GRCh37
NC_000005.8:g.155326811G= NCBI36
NG_008693.2:g.101880G= , LRG_205:g.101880G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96799G= ENSP00000429378.1:n.-282+96799G=
XM_017009723.2:c.-208+96799G= XP_016865212.1:n.-208+96799G=
XM_017009724.1:c.-207-156633G= XP_016865213.1:n.-207-156633G=