Canonical Allele Identifier: CA796086616

Gene: SGCB

Linked Data

• dbSNP Id: rs1485963633
• gnomAD v3: 4-52038370-C-T
• gnomAD v4: 4-52038370-C-T
• MyVariant Identifiers: chr4:g.52904536C>T (hg19) ; chr4:g.52038370C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038370C>T , CM000666.2:g.52038370C>T	GRCh38
NC_000004.11:g.52904536C>T , CM000666.1:g.52904536C>T	GRCh37
NC_000004.10:g.52599293C>T	NCBI36
NG_008891.1:g.4950G>A , LRG_204:g.4950G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.9:c.-111G>A	ENSP00000370839.5:n.-111G>A