Canonical Allele Identifier: CA551344230

Gene: SGCB

Linked Data

• dbSNP Id: rs1316975908
• gnomAD v2: 4-52904555-A-AGCCCGCATCCCTGACG
• gnomAD v3: 4-52038389-A-AGCCCGCATCCCTGACG
• gnomAD v4: 4-52038389-A-AGCCCGCATCCCTGACG
• MyVariant Identifiers: chr4:g.52904555_52904556insGCCCGCATCCCTGACG (hg19) ; chr4:g.52038389_52038390insGCCCGCATCCCTGACG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038390_52038405dup , CM000666.2:g.52038390_52038405dup	GRCh38
NC_000004.11:g.52904556_52904571dup , CM000666.1:g.52904556_52904571dup	GRCh37
NC_000004.10:g.52599313_52599328dup	NCBI36
NG_008891.1:g.4915_4930dup , LRG_204:g.4915_4930dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.9:c.-146_-131dup	ENSP00000370839.5:n.-146_-131dup