Canonical Allele Identifier: CA1457431651
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033267T= , CM000666.2:g.52033267T= GRCh38
NC_000004.11:g.52899433T= , CM000666.1:g.52899433T= GRCh37
NC_000004.10:g.52594190T= NCBI36
NG_008891.1:g.10053A= , LRG_204:g.10053A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.243+164A= MANE Select ENSP00000370839.6:n.243+164A=
ENST00000381431.9:c.243+164A= ENSP00000370839.5:n.243+164A=
ENST00000506357.5:c.229+164A=
ENST00000514133.1:c.210+164A= ENSP00000425818.1:n.210+164A=
NM_000232.4:c.243+164A= , LRG_204t1:c.243+164A= NP_000223.1:n.243+164A=
XM_006714049.2:c.-165+164A= XP_006714112.1:n.-165+164A=
XM_011534403.1:c.34-3404A= XP_011532705.1:n.34-3404A=
XM_011534404.1:c.-142+164A= XP_011532706.1:n.-142+164A=
NM_000232.5:c.243+164A= MANE Select NP_000223.1:n.243+164A=