Canonical Allele Identifier: CA2670614690

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038286-CCCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038291_52038294del , CM000666.2:g.52038291_52038294del	GRCh38
NC_000004.11:g.52904457_52904460del , CM000666.1:g.52904457_52904460del	GRCh37
NC_000004.10:g.52599214_52599217del	NCBI36
NG_008891.1:g.5030_5033del , LRG_204:g.5030_5033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.-31_-28del MANE Select	ENSP00000370839.6:n.-31_-28del
ENST00000381431.9:c.-31_-28del	ENSP00000370839.5:n.-31_-28del
NM_000232.4:c.-31_-28del , LRG_204t1:c.-31_-28del	NP_000223.1:n.-31_-28del
XM_011534403.1:c.-31_-28del	XP_011532705.1:n.-31_-28del
NM_000232.5:c.-31_-28del MANE Select	NP_000223.1:n.-31_-28del