Canonical Allele Identifier: CA2670614373

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038103-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038105_52038106del , CM000666.2:g.52038105_52038106del	GRCh38
NC_000004.11:g.52904271_52904272del , CM000666.1:g.52904271_52904272del	GRCh37
NC_000004.10:g.52599028_52599029del	NCBI36
NG_008891.1:g.5215_5216del , LRG_204:g.5215_5216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+122_33+123del MANE Select	ENSP00000370839.6:n.33+122_33+123del
ENST00000381431.9:c.33+122_33+123del	ENSP00000370839.5:n.33+122_33+123del
ENST00000506357.5:c.19+122_19+123del
NM_000232.4:c.33+122_33+123del , LRG_204t1:c.33+122_33+123del	NP_000223.1:n.33+122_33+123del
XM_011534403.1:c.33+122_33+123del	XP_011532705.1:n.33+122_33+123del
NM_000232.5:c.33+122_33+123del MANE Select	NP_000223.1:n.33+122_33+123del