Canonical Allele Identifier: CA1457434062
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038084_52038085delinsCG , CM000666.2:g.52038084_52038085delinsCG GRCh38
NC_000004.11:g.52904250_52904251delinsCG , CM000666.1:g.52904250_52904251delinsCG GRCh37
NC_000004.10:g.52599007_52599008delinsCG NCBI36
NG_008891.1:g.5235_5236delinsCG , LRG_204:g.5235_5236delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+142_33+143delinsCG MANE Select ENSP00000370839.6:n.33+142_33+143delinsCG
ENST00000381431.9:c.33+142_33+143delinsCG ENSP00000370839.5:n.33+142_33+143delinsCG
ENST00000506357.5:c.19+142_19+143delinsCG
NM_000232.4:c.33+142_33+143delinsCG , LRG_204t1:c.33+142_33+143delinsCG NP_000223.1:n.33+142_33+143delinsCG
XM_011534403.1:c.33+142_33+143delinsCG XP_011532705.1:n.33+142_33+143delinsCG
NM_000232.5:c.33+142_33+143delinsCG MANE Select NP_000223.1:n.33+142_33+143delinsCG