Canonical Allele Identifier: CA1062455003
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1560570614
gnomAD v3: 4-52038436-C-T
gnomAD v4: 4-52038436-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038436C>T , CM000666.2:g.52038436C>T GRCh38
NC_000004.11:g.52904602C>T , CM000666.1:g.52904602C>T GRCh37
NC_000004.10:g.52599359C>T NCBI36
NG_008891.1:g.4884G>A , LRG_204:g.4884G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-177G>A ENSP00000370839.5:n.-177G>A