Canonical Allele Identifier: CA1593483798

Gene: SGCD

Linked Data

• dbSNP Id: rs1757921446

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.155967295T>C , CM000667.2:g.155967295T>C	GRCh38
NC_000005.9:g.155394305T>C , CM000667.1:g.155394305T>C	GRCh37
NC_000005.8:g.155326883T>C	NCBI36
NG_008693.2:g.101952T>C , LRG_205:g.101952T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517913.5:c.-282+96871T>C	ENSP00000429378.1:n.-282+96871T>C
XM_017009723.2:c.-208+96871T>C	XP_016865212.1:n.-208+96871T>C
XM_017009724.1:c.-207-156561T>C	XP_016865213.1:n.-207-156561T>C