Canonical Allele Identifier: CA1457434266
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737460362
gnomAD v4: 4-52038335-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038335G>C , CM000666.2:g.52038335G>C GRCh38
NC_000004.11:g.52904501G>C , CM000666.1:g.52904501G>C GRCh37
NC_000004.10:g.52599258G>C NCBI36
NG_008891.1:g.4985C>G , LRG_204:g.4985C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-76C>G ENSP00000370839.5:n.-76C>G