Canonical Allele Identifier: CA1457431694
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033377G= , CM000666.2:g.52033377G= GRCh38
NC_000004.11:g.52899543G= , CM000666.1:g.52899543G= GRCh37
NC_000004.10:g.52594300G= NCBI36
NG_008891.1:g.9943C= , LRG_204:g.9943C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.243+54C= MANE Select ENSP00000370839.6:n.243+54C=
ENST00000381431.9:c.243+54C= ENSP00000370839.5:n.243+54C=
ENST00000506357.5:c.229+54C=
ENST00000514133.1:c.210+54C= ENSP00000425818.1:n.210+54C=
NM_000232.4:c.243+54C= , LRG_204t1:c.243+54C= NP_000223.1:n.243+54C=
XM_006714049.2:c.-165+54C= XP_006714112.1:n.-165+54C=
XM_011534403.1:c.34-3514C= XP_011532705.1:n.34-3514C=
XM_011534404.1:c.-142+54C= XP_011532706.1:n.-142+54C=
NM_000232.5:c.243+54C= MANE Select NP_000223.1:n.243+54C=