Canonical Allele Identifier: CA796086675

Gene: SGCB

Linked Data

• dbSNP Id: rs1166723255
• MyVariant Identifiers: chr4:g.52904585_52904611del (hg19) ; chr4:g.52038419_52038445del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038425_52038451del , CM000666.2:g.52038425_52038451del	GRCh38
NC_000004.11:g.52904591_52904617del , CM000666.1:g.52904591_52904617del	GRCh37
NC_000004.10:g.52599348_52599374del	NCBI36
NG_008891.1:g.4875_4901del , LRG_204:g.4875_4901del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.9:c.-186_-160del	ENSP00000370839.5:n.-186_-160del