Canonical Allele Identifier: CA2078571305
Gene: SGCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23170240C= , CM000675.2:g.23170240C= GRCh38
NC_000013.10:g.23744379C= , CM000675.1:g.23744379C= GRCh37
NC_000013.9:g.22642379C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_006719861.2:c.54+9594C= XP_006719924.1:n.54+9594C=
XM_006719861.3:c.54+9594C= XP_006719924.1:n.54+9594C=
NM_001378244.1:c.54+9594C= NP_001365173.1:n.54+9594C=