Canonical Allele Identifier: CA130528121

Gene: SGCD

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.155775518A>G , CM000667.2:g.155775518A>G	GRCh38
NC_000005.9:g.155202528A>G , CM000667.1:g.155202528A>G	GRCh37
NC_000005.8:g.155135106A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017009724.1:c.-208+46528A>G	XP_016865213.1:n.-208+46528A>G