Canonical Allele Identifier: CA2670614251

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038076-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038076_52038077insTG , CM000666.2:g.52038076_52038077insTG	GRCh38
NC_000004.11:g.52904242_52904243insTG , CM000666.1:g.52904242_52904243insTG	GRCh37
NC_000004.10:g.52598999_52599000insTG	NCBI36
NG_008891.1:g.5243_5244insCA , LRG_204:g.5243_5244insCA

Transcript Alleles

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