Canonical Allele Identifier: CA796086558

Gene: SGCB

Linked Data

• dbSNP Id: rs1378869404
• MyVariant Identifiers: chr4:g.52904493G>C (hg19) ; chr4:g.52038327G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038327G>C , CM000666.2:g.52038327G>C	GRCh38
NC_000004.11:g.52904493G>C , CM000666.1:g.52904493G>C	GRCh37
NC_000004.10:g.52599250G>C	NCBI36
NG_008891.1:g.4993C>G , LRG_204:g.4993C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.9:c.-68C>G	ENSP00000370839.5:n.-68C>G