Canonical Allele Identifier: CA2670614301

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038087-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038087_52038088insG , CM000666.2:g.52038087_52038088insG	GRCh38
NC_000004.11:g.52904253_52904254insG , CM000666.1:g.52904253_52904254insG	GRCh37
NC_000004.10:g.52599010_52599011insG	NCBI36
NG_008891.1:g.5232_5233insC , LRG_204:g.5232_5233insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+139_33+140insC MANE Select	ENSP00000370839.6:n.33+139_33+140insC
ENST00000381431.9:c.33+139_33+140insC	ENSP00000370839.5:n.33+139_33+140insC
ENST00000506357.5:c.19+139_19+140insC
NM_000232.4:c.33+139_33+140insC , LRG_204t1:c.33+139_33+140insC	NP_000223.1:n.33+139_33+140insC
XM_011534403.1:c.33+139_33+140insC	XP_011532705.1:n.33+139_33+140insC
NM_000232.5:c.33+139_33+140insC MANE Select	NP_000223.1:n.33+139_33+140insC