Canonical Allele Identifier: CA2670598597
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027885del , CM000666.2:g.52027885del GRCh38
NC_000004.11:g.52894051del , CM000666.1:g.52894051del GRCh37
NC_000004.10:g.52588808del NCBI36
NG_008891.1:g.15438del , LRG_204:g.15438del

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+86del MANE Select ENSP00000370839.6:n.753+86del
ENST00000381431.9:c.753+86del ENSP00000370839.5:n.753+86del
NM_000232.4:c.753+86del , LRG_204t1:c.753+86del NP_000223.1:n.753+86del
XM_006714049.2:c.456+86del XP_006714112.1:n.456+86del
XM_011534403.1:c.543+86del XP_011532705.1:n.543+86del
XM_011534404.1:c.456+86del XP_011532706.1:n.456+86del
NM_000232.5:c.753+86del MANE Select NP_000223.1:n.753+86del