Canonical Allele Identifier: CA2078571255
Gene: SGCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23170146A= , CM000675.2:g.23170146A= GRCh38
NC_000013.10:g.23744285A= , CM000675.1:g.23744285A= GRCh37
NC_000013.9:g.22642285A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_006719861.2:c.54+9500A= XP_006719924.1:n.54+9500A=
XM_006719861.3:c.54+9500A= XP_006719924.1:n.54+9500A=
NM_001378244.1:c.54+9500A= NP_001365173.1:n.54+9500A=