Canonical Allele Identifier: CA2670614353

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038097-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038097_52038098insG , CM000666.2:g.52038097_52038098insG	GRCh38
NC_000004.11:g.52904263_52904264insG , CM000666.1:g.52904263_52904264insG	GRCh37
NC_000004.10:g.52599020_52599021insG	NCBI36
NG_008891.1:g.5222_5223insC , LRG_204:g.5222_5223insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+129_33+130insC MANE Select	ENSP00000370839.6:n.33+129_33+130insC
ENST00000381431.9:c.33+129_33+130insC	ENSP00000370839.5:n.33+129_33+130insC
ENST00000506357.5:c.19+129_19+130insC
NM_000232.4:c.33+129_33+130insC , LRG_204t1:c.33+129_33+130insC	NP_000223.1:n.33+129_33+130insC
XM_011534403.1:c.33+129_33+130insC	XP_011532705.1:n.33+129_33+130insC
NM_000232.5:c.33+129_33+130insC MANE Select	NP_000223.1:n.33+129_33+130insC