Canonical Allele Identifier: CA2670614662

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038272-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038274dup , CM000666.2:g.52038274dup	GRCh38
NC_000004.11:g.52904440dup , CM000666.1:g.52904440dup	GRCh37
NC_000004.10:g.52599197dup	NCBI36
NG_008891.1:g.5047dup , LRG_204:g.5047dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.-14dup MANE Select	ENSP00000370839.6:n.-14dup
ENST00000381431.9:c.-14dup	ENSP00000370839.5:n.-14dup
NM_000232.4:c.-14dup , LRG_204t1:c.-14dup	NP_000223.1:n.-14dup
XM_011534403.1:c.-14dup	XP_011532705.1:n.-14dup
NM_000232.5:c.-14dup MANE Select	NP_000223.1:n.-14dup