Canonical Allele Identifier: CA2761648127

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038075_52038076insGG , CM000666.2:g.52038075_52038076insGG	GRCh38
NC_000004.11:g.52904241_52904242insGG , CM000666.1:g.52904241_52904242insGG	GRCh37
NC_000004.10:g.52598998_52598999insGG	NCBI36
NG_008891.1:g.5244_5245insCC , LRG_204:g.5244_5245insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+151_33+152insCC MANE Select	ENSP00000370839.6:n.33+151_33+152insCC
ENST00000381431.9:c.33+151_33+152insCC	ENSP00000370839.5:n.33+151_33+152insCC
ENST00000506357.5:c.19+151_19+152insCC
NM_000232.4:c.33+151_33+152insCC , LRG_204t1:c.33+151_33+152insCC	NP_000223.1:n.33+151_33+152insCC
XM_011534403.1:c.33+151_33+152insCC	XP_011532705.1:n.33+151_33+152insCC
NM_000232.5:c.33+151_33+152insCC MANE Select	NP_000223.1:n.33+151_33+152insCC