Canonical Allele Identifier: CA2705877331
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs2109381249

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038413T>C , CM000666.2:g.52038413T>C GRCh38
NC_000004.11:g.52904579T>C , CM000666.1:g.52904579T>C GRCh37
NC_000004.10:g.52599336T>C NCBI36
NG_008891.1:g.4907A>G , LRG_204:g.4907A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-154A>G ENSP00000370839.5:n.-154A>G