Canonical Allele Identifier: CA2670614395
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038115_52038116del , CM000666.2:g.52038115_52038116del GRCh38
NC_000004.11:g.52904281_52904282del , CM000666.1:g.52904281_52904282del GRCh37
NC_000004.10:g.52599038_52599039del NCBI36
NG_008891.1:g.5205_5206del , LRG_204:g.5205_5206del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+112_33+113del MANE Select ENSP00000370839.6:n.33+112_33+113del
ENST00000381431.9:c.33+112_33+113del ENSP00000370839.5:n.33+112_33+113del
ENST00000506357.5:c.19+112_19+113del
NM_000232.4:c.33+112_33+113del , LRG_204t1:c.33+112_33+113del NP_000223.1:n.33+112_33+113del
XM_011534403.1:c.33+112_33+113del XP_011532705.1:n.33+112_33+113del
NM_000232.5:c.33+112_33+113del MANE Select NP_000223.1:n.33+112_33+113del