Canonical Allele Identifier: CA2555798854

Gene: SGCB

Linked Data

• dbSNP Id: rs2109369770
• gnomAD v4: 4-52027858-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52027859dup , CM000666.2:g.52027859dup	GRCh38
NC_000004.11:g.52894025dup , CM000666.1:g.52894025dup	GRCh37
NC_000004.10:g.52588782dup	NCBI36
NG_008891.1:g.15461dup , LRG_204:g.15461dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.753+109dup MANE Select	ENSP00000370839.6:n.753+109dup
ENST00000381431.9:c.753+109dup	ENSP00000370839.5:n.753+109dup
NM_000232.4:c.753+109dup , LRG_204t1:c.753+109dup	NP_000223.1:n.753+109dup
XM_006714049.2:c.456+109dup	XP_006714112.1:n.456+109dup
XM_011534403.1:c.543+109dup	XP_011532705.1:n.543+109dup
XM_011534404.1:c.456+109dup	XP_011532706.1:n.456+109dup
NM_000232.5:c.753+109dup MANE Select	NP_000223.1:n.753+109dup