Canonical Allele Identifier: CA2670614249

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038076-T-TGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038076_52038077insGGCC , CM000666.2:g.52038076_52038077insGGCC	GRCh38
NC_000004.11:g.52904242_52904243insGGCC , CM000666.1:g.52904242_52904243insGGCC	GRCh37
NC_000004.10:g.52598999_52599000insGGCC	NCBI36
NG_008891.1:g.5243_5244insGGCC , LRG_204:g.5243_5244insGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+150_33+151insGGCC MANE Select	ENSP00000370839.6:n.33+150_33+151insGGCC
ENST00000381431.9:c.33+150_33+151insGGCC	ENSP00000370839.5:n.33+150_33+151insGGCC
ENST00000506357.5:c.19+150_19+151insGGCC
NM_000232.4:c.33+150_33+151insGGCC , LRG_204t1:c.33+150_33+151insGGCC	NP_000223.1:n.33+150_33+151insGGCC
XM_011534403.1:c.33+150_33+151insGGCC	XP_011532705.1:n.33+150_33+151insGGCC
NM_000232.5:c.33+150_33+151insGGCC MANE Select	NP_000223.1:n.33+150_33+151insGGCC