Canonical Allele Identifier: CA2670614697
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038289-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038290del , CM000666.2:g.52038290del GRCh38
NC_000004.11:g.52904456del , CM000666.1:g.52904456del GRCh37
NC_000004.10:g.52599213del NCBI36
NG_008891.1:g.5030del , LRG_204:g.5030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-31del MANE Select ENSP00000370839.6:n.-31del
ENST00000381431.9:c.-31del ENSP00000370839.5:n.-31del
NM_000232.4:c.-31del , LRG_204t1:c.-31del NP_000223.1:n.-31del
XM_011534403.1:c.-31del XP_011532705.1:n.-31del
NM_000232.5:c.-31del MANE Select NP_000223.1:n.-31del
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