Canonical Allele Identifier: CA2670614262

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038076-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038078_52038079dup , CM000666.2:g.52038078_52038079dup	GRCh38
NC_000004.11:g.52904244_52904245dup , CM000666.1:g.52904244_52904245dup	GRCh37
NC_000004.10:g.52599001_52599002dup	NCBI36
NG_008891.1:g.5242_5243dup , LRG_204:g.5242_5243dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+149_33+150dup MANE Select	ENSP00000370839.6:n.33+149_33+150dup
ENST00000381431.9:c.33+149_33+150dup	ENSP00000370839.5:n.33+149_33+150dup
ENST00000506357.5:c.19+149_19+150dup
NM_000232.4:c.33+149_33+150dup , LRG_204t1:c.33+149_33+150dup	NP_000223.1:n.33+149_33+150dup
XM_011534403.1:c.33+149_33+150dup	XP_011532705.1:n.33+149_33+150dup
NM_000232.5:c.33+149_33+150dup MANE Select	NP_000223.1:n.33+149_33+150dup