Canonical Allele Identifier: CA2670598694
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52028219-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028223del , CM000666.2:g.52028223del GRCh38
NC_000004.11:g.52894389del , CM000666.1:g.52894389del GRCh37
NC_000004.10:g.52589146del NCBI36
NG_008891.1:g.15100del , LRG_204:g.15100del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.622-121del MANE Select ENSP00000370839.6:n.622-121del
ENST00000381431.9:c.622-121del ENSP00000370839.5:n.622-121del
NM_000232.4:c.622-121del , LRG_204t1:c.622-121del NP_000223.1:n.622-121del
XM_006714049.2:c.325-121del XP_006714112.1:n.325-121del
XM_011534403.1:c.412-121del XP_011532705.1:n.412-121del
XM_011534404.1:c.325-121del XP_011532706.1:n.325-121del
NM_000232.5:c.622-121del MANE Select NP_000223.1:n.622-121del
Search 100 bp 5'
Search 100 bp 3'