Canonical Allele Identifier: CA96791884

Gene: SGCB

Linked Data

• dbSNP Id: rs961510186
• gnomAD v4: 4-52038422-T-G
• MyVariant Identifiers: chr4:g.52904588T>G (hg19) ; chr4:g.52038422T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038422T>G , CM000666.2:g.52038422T>G	GRCh38
NC_000004.11:g.52904588T>G , CM000666.1:g.52904588T>G	GRCh37
NC_000004.10:g.52599345T>G	NCBI36
NG_008891.1:g.4898A>C , LRG_204:g.4898A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.9:c.-163A>C	ENSP00000370839.5:n.-163A>C