Canonical Allele Identifier: CA1457434367
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737466806

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038476G>C , CM000666.2:g.52038476G>C GRCh38
NC_000004.11:g.52904642G>C , CM000666.1:g.52904642G>C GRCh37
NC_000004.10:g.52599399G>C NCBI36
NG_008891.1:g.4844C>G , LRG_204:g.4844C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-217C>G ENSP00000370839.5:n.-217C>G