Canonical Allele Identifier: CA1457434141
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038184_52038185delinsTC , CM000666.2:g.52038184_52038185delinsTC GRCh38
NC_000004.11:g.52904350_52904351delinsTC , CM000666.1:g.52904350_52904351delinsTC GRCh37
NC_000004.10:g.52599107_52599108delinsTC NCBI36
NG_008891.1:g.5135_5136delinsGA , LRG_204:g.5135_5136delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+42_33+43delinsGA MANE Select ENSP00000370839.6:n.33+42_33+43delinsGA
ENST00000381431.9:c.33+42_33+43delinsGA ENSP00000370839.5:n.33+42_33+43delinsGA
ENST00000506357.5:c.19+42_19+43delinsGA
NM_000232.4:c.33+42_33+43delinsGA , LRG_204t1:c.33+42_33+43delinsGA NP_000223.1:n.33+42_33+43delinsGA
XM_011534403.1:c.33+42_33+43delinsGA XP_011532705.1:n.33+42_33+43delinsGA
NM_000232.5:c.33+42_33+43delinsGA MANE Select NP_000223.1:n.33+42_33+43delinsGA