Canonical Allele Identifier: CA1457431781
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033589T= , CM000666.2:g.52033589T= GRCh38
NC_000004.11:g.52899755T= , CM000666.1:g.52899755T= GRCh37
NC_000004.10:g.52594512T= NCBI36
NG_008891.1:g.9731A= , LRG_204:g.9731A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.85A= MANE Select ENSP00000370839.6:p.Arg29=
ENST00000381431.9:c.85A= ENSP00000370839.5:p.Arg29=
ENST00000506357.5:c.71A=
ENST00000514133.1:c.52A= ENSP00000425818.1:p.Arg18=
NM_000232.4:c.85A= , LRG_204t1:c.85A= NP_000223.1:p.Arg29=
XM_011534403.1:c.34-3726A= XP_011532705.1:n.34-3726A=
NM_000232.5:c.85A= MANE Select NP_000223.1:p.Arg29=