Canonical Allele Identifier: CA2670614365

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038098-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038098_52038099insAG , CM000666.2:g.52038098_52038099insAG	GRCh38
NC_000004.11:g.52904264_52904265insAG , CM000666.1:g.52904264_52904265insAG	GRCh37
NC_000004.10:g.52599021_52599022insAG	NCBI36
NG_008891.1:g.5221_5222insCT , LRG_204:g.5221_5222insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+128_33+129insCT MANE Select	ENSP00000370839.6:n.33+128_33+129insCT
ENST00000381431.9:c.33+128_33+129insCT	ENSP00000370839.5:n.33+128_33+129insCT
ENST00000506357.5:c.19+128_19+129insCT
NM_000232.4:c.33+128_33+129insCT , LRG_204t1:c.33+128_33+129insCT	NP_000223.1:n.33+128_33+129insCT
XM_011534403.1:c.33+128_33+129insCT	XP_011532705.1:n.33+128_33+129insCT
NM_000232.5:c.33+128_33+129insCT MANE Select	NP_000223.1:n.33+128_33+129insCT