Canonical Allele Identifier: CA1457429038
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737139769

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027821_52027822insAGCACGCCCATCAA , CM000666.2:g.52027821_52027822insAGCACGCCCATCAA GRCh38
NC_000004.11:g.52893987_52893988insAGCACGCCCATCAA , CM000666.1:g.52893987_52893988insAGCACGCCCATCAA GRCh37
NC_000004.10:g.52588744_52588745insAGCACGCCCATCAA NCBI36
NG_008891.1:g.15498_15499insTTGATGGGCGTGCT , LRG_204:g.15498_15499insTTGATGGGCGTGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+146_753+147insTTGATGGGCGTGCT MANE Select ENSP00000370839.6:n.753+146_753+147insTTG...
ENST00000381431.9:c.753+146_753+147insTTGATGGGCGTGCT ENSP00000370839.5:n.753+146_753+147insTTG...
NM_000232.4:c.753+146_753+147insTTGATGGGCGTGCT , LRG_204t1:c.753+146_753+147insTTGATGGGCGTGCT NP_000223.1:n.753+146_753+147insTTGATGGGC...
XM_006714049.2:c.456+146_456+147insTTGATGGGCGTGCT XP_006714112.1:n.456+146_456+147insTTGATG...
XM_011534403.1:c.543+146_543+147insTTGATGGGCGTGCT XP_011532705.1:n.543+146_543+147insTTGATG...
XM_011534404.1:c.456+146_456+147insTTGATGGGCGTGCT XP_011532706.1:n.456+146_456+147insTTGATG...
NM_000232.5:c.753+146_753+147insTTGATGGGCGTGCT MANE Select NP_000223.1:n.753+146_753+147insTTGATGGGC...