Canonical Allele Identifier: CA806083459
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs1023324011

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967271G>A , CM000667.2:g.155967271G>A GRCh38
NC_000005.9:g.155394281G>A , CM000667.1:g.155394281G>A GRCh37
NC_000005.8:g.155326859G>A NCBI36
NG_008693.2:g.101928G>A , LRG_205:g.101928G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96847G>A ENSP00000429378.1:n.-282+96847G>A
XM_017009723.2:c.-208+96847G>A XP_016865212.1:n.-208+96847G>A
XM_017009724.1:c.-207-156585G>A XP_016865213.1:n.-207-156585G>A