Canonical Allele Identifier: CA1593468235
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155924251T= , CM000667.2:g.155924251T= GRCh38
NC_000005.9:g.155351261T= , CM000667.1:g.155351261T= GRCh37
NC_000005.8:g.155283839T= NCBI36
NG_008693.2:g.58908T= , LRG_205:g.58908T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+53827T= ENSP00000429378.1:n.-282+53827T=
XM_017009723.2:c.-208+53827T= XP_016865212.1:n.-208+53827T=
XM_017009724.1:c.-208+195261T= XP_016865213.1:n.-208+195261T=