Canonical Allele Identifier: CA12013786

Gene: SGCD

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156218241G>A , CM000667.2:g.156218241G>A	GRCh38
NC_000005.9:g.155645251G>A , CM000667.1:g.155645251G>A	GRCh37
NC_000005.8:g.155577829G>A	NCBI36
NG_008693.2:g.352898G>A , LRG_205:g.352898G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517913.5:c.-44+94222G>A	ENSP00000429378.1:n.-44+94222G>A
XM_006714911.2:c.-44+94222G>A	XP_006714974.1:n.-44+94222G>A
XM_011534621.1:c.-1+94222G>A	XP_011532923.1:n.-1+94222G>A
XM_011534621.2:c.-1+94222G>A	XP_011532923.1:n.-1+94222G>A
XM_017009723.2:c.-44+94222G>A	XP_016865212.1:n.-44+94222G>A
XM_017009724.1:c.-44+94222G>A	XP_016865213.1:n.-44+94222G>A