Canonical Allele Identifier: CA1457431745
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033515G= , CM000666.2:g.52033515G= GRCh38
NC_000004.11:g.52899681G= , CM000666.1:g.52899681G= GRCh37
NC_000004.10:g.52594438G= NCBI36
NG_008891.1:g.9805C= , LRG_204:g.9805C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.159C= MANE Select ENSP00000370839.6:p.His53=
ENST00000381431.9:c.159C= ENSP00000370839.5:p.His53=
ENST00000506357.5:c.145C=
ENST00000514133.1:c.126C= ENSP00000425818.1:p.His42=
NM_000232.4:c.159C= , LRG_204t1:c.159C= NP_000223.1:p.His53=
XM_006714049.2:c.-249C= XP_006714112.1:n.-249C=
XM_011534403.1:c.34-3652C= XP_011532705.1:n.34-3652C=
XM_011534404.1:c.-226C= XP_011532706.1:n.-226C=
NM_000232.5:c.159C= MANE Select NP_000223.1:p.His53=