Canonical Allele Identifier: CA1062455034
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737466017
gnomAD v3: 4-52038461-C-G
gnomAD v4: 4-52038461-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038461C>G , CM000666.2:g.52038461C>G GRCh38
NC_000004.11:g.52904627C>G , CM000666.1:g.52904627C>G GRCh37
NC_000004.10:g.52599384C>G NCBI36
NG_008891.1:g.4859G>C , LRG_204:g.4859G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-202G>C ENSP00000370839.5:n.-202G>C