Canonical Allele Identifier: CA2670614308

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038088-C-CCCCCCCCCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038089_52038090insCCCCCCCAAC , CM000666.2:g.52038089_52038090insCCCCCCCAAC	GRCh38
NC_000004.11:g.52904255_52904256insCCCCCCCAAC , CM000666.1:g.52904255_52904256insCCCCCCCAAC	GRCh37
NC_000004.10:g.52599012_52599013insCCCCCCCAAC	NCBI36
NG_008891.1:g.5231_5232insTTGGGGGGGG , LRG_204:g.5231_5232insTTGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+138_33+139insTTGGGGGGGG MANE Select	ENSP00000370839.6:n.33+138_33+139insTTGGGGGGGG
ENST00000381431.9:c.33+138_33+139insTTGGGGGGGG	ENSP00000370839.5:n.33+138_33+139insTTGGGGGGGG
ENST00000506357.5:c.19+138_19+139insTTGGGGGGGG
NM_000232.4:c.33+138_33+139insTTGGGGGGGG , LRG_204t1:c.33+138_33+139insTTGGGGGGGG	NP_000223.1:n.33+138_33+139insTTGGGGGGGG
XM_011534403.1:c.33+138_33+139insTTGGGGGGGG	XP_011532705.1:n.33+138_33+139insTTGGGGGGGG
NM_000232.5:c.33+138_33+139insTTGGGGGGGG MANE Select	NP_000223.1:n.33+138_33+139insTTGGGGGGGG