Canonical Allele Identifier: CA1593483774
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967242G= , CM000667.2:g.155967242G= GRCh38
NC_000005.9:g.155394252G= , CM000667.1:g.155394252G= GRCh37
NC_000005.8:g.155326830G= NCBI36
NG_008693.2:g.101899G= , LRG_205:g.101899G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96818G= ENSP00000429378.1:n.-282+96818G=
XM_017009723.2:c.-208+96818G= XP_016865212.1:n.-208+96818G=
XM_017009724.1:c.-207-156614G= XP_016865213.1:n.-207-156614G=