Canonical Allele Identifier: CA1457431738
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033486T= , CM000666.2:g.52033486T= GRCh38
NC_000004.11:g.52899652T= , CM000666.1:g.52899652T= GRCh37
NC_000004.10:g.52594409T= NCBI36
NG_008891.1:g.9834A= , LRG_204:g.9834A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.188A= MANE Select ENSP00000370839.6:p.Asn63=
ENST00000381431.9:c.188A= ENSP00000370839.5:p.Asn63=
ENST00000506357.5:c.174A=
ENST00000514133.1:c.155A= ENSP00000425818.1:p.Asn52=
NM_000232.4:c.188A= , LRG_204t1:c.188A= NP_000223.1:p.Asn63=
XM_006714049.2:c.-220A= XP_006714112.1:n.-220A=
XM_011534403.1:c.34-3623A= XP_011532705.1:n.34-3623A=
XM_011534404.1:c.-197A= XP_011532706.1:n.-197A=
NM_000232.5:c.188A= MANE Select NP_000223.1:p.Asn63=