Canonical Allele Identifier: CA2761641244
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027875_52027879del , CM000666.2:g.52027875_52027879del GRCh38
NC_000004.11:g.52894041_52894045del , CM000666.1:g.52894041_52894045del GRCh37
NC_000004.10:g.52588798_52588802del NCBI36
NG_008891.1:g.15443_15447del , LRG_204:g.15443_15447del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.753+91_753+95del MANE Select ENSP00000370839.6:n.753+91_753+95del
ENST00000381431.9:c.753+91_753+95del ENSP00000370839.5:n.753+91_753+95del
NM_000232.4:c.753+91_753+95del , LRG_204t1:c.753+91_753+95del NP_000223.1:n.753+91_753+95del
XM_006714049.2:c.456+91_456+95del XP_006714112.1:n.456+91_456+95del
XM_011534403.1:c.543+91_543+95del XP_011532705.1:n.543+91_543+95del
XM_011534404.1:c.456+91_456+95del XP_011532706.1:n.456+91_456+95del
NM_000232.5:c.753+91_753+95del MANE Select NP_000223.1:n.753+91_753+95del