Canonical Allele Identifier: CA1457429068
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737141518

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027867del , CM000666.2:g.52027867del GRCh38
NC_000004.11:g.52894033del , CM000666.1:g.52894033del GRCh37
NC_000004.10:g.52588790del NCBI36
NG_008891.1:g.15453del , LRG_204:g.15453del

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+101del MANE Select ENSP00000370839.6:n.753+101del
ENST00000381431.9:c.753+101del ENSP00000370839.5:n.753+101del
NM_000232.4:c.753+101del , LRG_204t1:c.753+101del NP_000223.1:n.753+101del
XM_006714049.2:c.456+101del XP_006714112.1:n.456+101del
XM_011534403.1:c.543+101del XP_011532705.1:n.543+101del
XM_011534404.1:c.456+101del XP_011532706.1:n.456+101del
NM_000232.5:c.753+101del MANE Select NP_000223.1:n.753+101del