Canonical Allele Identifier: CA1457434303
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737461748

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038376C>G , CM000666.2:g.52038376C>G GRCh38
NC_000004.11:g.52904542C>G , CM000666.1:g.52904542C>G GRCh37
NC_000004.10:g.52599299C>G NCBI36
NG_008891.1:g.4944G>C , LRG_204:g.4944G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-117G>C ENSP00000370839.5:n.-117G>C