Canonical Allele Identifier: CA2556478867

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038113_52038114insCCCC , CM000666.2:g.52038113_52038114insCCCC	GRCh38
NC_000004.11:g.52904279_52904280insCCCC , CM000666.1:g.52904279_52904280insCCCC	GRCh37
NC_000004.10:g.52599036_52599037insCCCC	NCBI36
NG_008891.1:g.5209_5210insGGGG , LRG_204:g.5209_5210insGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+116_33+117insGGGG MANE Select	ENSP00000370839.6:n.33+116_33+117insGGGG
ENST00000381431.9:c.33+116_33+117insGGGG	ENSP00000370839.5:n.33+116_33+117insGGGG
ENST00000506357.5:c.19+116_19+117insGGGG
NM_000232.4:c.33+116_33+117insGGGG , LRG_204t1:c.33+116_33+117insGGGG	NP_000223.1:n.33+116_33+117insGGGG
XM_011534403.1:c.33+116_33+117insGGGG	XP_011532705.1:n.33+116_33+117insGGGG
NM_000232.5:c.33+116_33+117insGGGG MANE Select	NP_000223.1:n.33+116_33+117insGGGG