Canonical Allele Identifier: CA1457434249
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1578130135

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038317C>G , CM000666.2:g.52038317C>G GRCh38
NC_000004.11:g.52904483C>G , CM000666.1:g.52904483C>G GRCh37
NC_000004.10:g.52599240C>G NCBI36
NG_008891.1:g.5003G>C , LRG_204:g.5003G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-58G>C ENSP00000370839.5:n.-58G>C
NM_000232.4:c.-58G>C , LRG_204t1:c.-58G>C NP_000223.1:n.-58G>C