Canonical Allele Identifier: CA1457431723
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033436A= , CM000666.2:g.52033436A= GRCh38
NC_000004.11:g.52899602A= , CM000666.1:g.52899602A= GRCh37
NC_000004.10:g.52594359A= NCBI36
NG_008891.1:g.9884T= , LRG_204:g.9884T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.238T= MANE Select ENSP00000370839.6:p.Leu80=
ENST00000381431.9:c.238T= ENSP00000370839.5:p.Leu80=
ENST00000506357.5:c.224T=
ENST00000514133.1:c.205T= ENSP00000425818.1:p.Leu69=
NM_000232.4:c.238T= , LRG_204t1:c.238T= NP_000223.1:p.Leu80=
XM_006714049.2:c.-170T= XP_006714112.1:n.-170T=
XM_011534403.1:c.34-3573T= XP_011532705.1:n.34-3573T=
XM_011534404.1:c.-147T= XP_011532706.1:n.-147T=
NM_000232.5:c.238T= MANE Select NP_000223.1:p.Leu80=