Canonical Allele Identifier: CA2670614653

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038268-G-GCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038269_52038271dup , CM000666.2:g.52038269_52038271dup	GRCh38
NC_000004.11:g.52904435_52904437dup , CM000666.1:g.52904435_52904437dup	GRCh37
NC_000004.10:g.52599192_52599194dup	NCBI36
NG_008891.1:g.5049_5051dup , LRG_204:g.5049_5051dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.-12_-10dup MANE Select	ENSP00000370839.6:n.-12_-10dup
ENST00000381431.9:c.-12_-10dup	ENSP00000370839.5:n.-12_-10dup
NM_000232.4:c.-12_-10dup , LRG_204t1:c.-12_-10dup	NP_000223.1:n.-12_-10dup
XM_011534403.1:c.-12_-10dup	XP_011532705.1:n.-12_-10dup
NM_000232.5:c.-12_-10dup MANE Select	NP_000223.1:n.-12_-10dup