Canonical Allele Identifier: CA2670598635

Gene: SGCB

Linked Data

• gnomAD v4: 4-52028100-C-CCTTTCAGTAGATGCCTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028100_52028101insCTTTCAGTAGATGCCTTT , CM000666.2:g.52028100_52028101insCTTTCAGTAGATGCCTTT	GRCh38
NC_000004.11:g.52894266_52894267insCTTTCAGTAGATGCCTTT , CM000666.1:g.52894266_52894267insCTTTCAGTAGATGCCTTT	GRCh37
NC_000004.10:g.52589023_52589024insCTTTCAGTAGATGCCTTT	NCBI36
NG_008891.1:g.15219_15220insAAAGGCATCTACTGAAAG , LRG_204:g.15219_15220insAAAGGCATCTACTGAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.622-2_622-1insAAAGGCATCTACTGAAAG MANE Select	ENSP00000370839.6:n.622-2_622-1insAAAGGCATCTACTGAAAG
ENST00000381431.9:c.622-2_622-1insAAAGGCATCTACTGAAAG	ENSP00000370839.5:n.622-2_622-1insAAAGGCATCTACTGAAAG
NM_000232.4:c.622-2_622-1insAAAGGCATCTACTGAAAG , LRG_204t1:c.622-2_622-1insAAAGGCATCTACTGAAAG	NP_000223.1:n.622-2_622-1insAAAGGCATCTACTGAAAG
XM_006714049.2:c.325-2_325-1insAAAGGCATCTACTGAAAG	XP_006714112.1:n.325-2_325-1insAAAGGCATCTACTGAAAG
XM_011534403.1:c.412-2_412-1insAAAGGCATCTACTGAAAG	XP_011532705.1:n.412-2_412-1insAAAGGCATCTACTGAAAG
XM_011534404.1:c.325-2_325-1insAAAGGCATCTACTGAAAG	XP_011532706.1:n.325-2_325-1insAAAGGCATCTACTGAAAG
NM_000232.5:c.622-2_622-1insAAAGGCATCTACTGAAAG MANE Select	NP_000223.1:n.622-2_622-1insAAAGGCATCTACTGAAAG