Canonical Allele Identifier: CA1593483783
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967261A= , CM000667.2:g.155967261A= GRCh38
NC_000005.9:g.155394271A= , CM000667.1:g.155394271A= GRCh37
NC_000005.8:g.155326849A= NCBI36
NG_008693.2:g.101918A= , LRG_205:g.101918A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96837A= ENSP00000429378.1:n.-282+96837A=
XM_017009723.2:c.-208+96837A= XP_016865212.1:n.-208+96837A=
XM_017009724.1:c.-207-156595A= XP_016865213.1:n.-207-156595A=