Canonical Allele Identifier: CA1457431782
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033591T= , CM000666.2:g.52033591T= GRCh38
NC_000004.11:g.52899757T= , CM000666.1:g.52899757T= GRCh37
NC_000004.10:g.52594514T= NCBI36
NG_008891.1:g.9729A= , LRG_204:g.9729A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.83A= MANE Select ENSP00000370839.6:p.Glu28=
ENST00000381431.9:c.83A= ENSP00000370839.5:p.Glu28=
ENST00000506357.5:c.69A=
ENST00000514133.1:c.50A= ENSP00000425818.1:p.Glu17=
NM_000232.4:c.83A= , LRG_204t1:c.83A= NP_000223.1:p.Glu28=
XM_011534403.1:c.34-3728A= XP_011532705.1:n.34-3728A=
NM_000232.5:c.83A= MANE Select NP_000223.1:p.Glu28=