Canonical Allele Identifier: CA2670614295

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038084-C-CCCCCCCCCCCCCAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038084_52038085insCCCCCCCCCCCCAAA , CM000666.2:g.52038084_52038085insCCCCCCCCCCCCAAA	GRCh38
NC_000004.11:g.52904250_52904251insCCCCCCCCCCCCAAA , CM000666.1:g.52904250_52904251insCCCCCCCCCCCCAAA	GRCh37
NC_000004.10:g.52599007_52599008insCCCCCCCCCCCCAAA	NCBI36
NG_008891.1:g.5235_5236insTTTGGGGGGGGGGGG , LRG_204:g.5235_5236insTTTGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.33+142_33+143insTTTGGGGGGGGGGGG MANE Select	ENSP00000370839.6:n.33+142_33+143insTTTGGGGGGGGGGGG
ENST00000381431.9:c.33+142_33+143insTTTGGGGGGGGGGGG	ENSP00000370839.5:n.33+142_33+143insTTTGGGGGGGGGGGG
ENST00000506357.5:c.19+142_19+143insTTTGGGGGGGGGGGG
NM_000232.4:c.33+142_33+143insTTTGGGGGGGGGGGG , LRG_204t1:c.33+142_33+143insTTTGGGGGGGGGGGG	NP_000223.1:n.33+142_33+143insTTTGGGGGGGGGGGG
XM_011534403.1:c.33+142_33+143insTTTGGGGGGGGGGGG	XP_011532705.1:n.33+142_33+143insTTTGGGGGGGGGGGG
NM_000232.5:c.33+142_33+143insTTTGGGGGGGGGGGG MANE Select	NP_000223.1:n.33+142_33+143insTTTGGGGGGGGGGGG