Canonical Allele Identifier: CA1457431700
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033394C= , CM000666.2:g.52033394C= GRCh38
NC_000004.11:g.52899560C= , CM000666.1:g.52899560C= GRCh37
NC_000004.10:g.52594317C= NCBI36
NG_008891.1:g.9926G= , LRG_204:g.9926G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.243+37G= MANE Select ENSP00000370839.6:n.243+37G=
ENST00000381431.9:c.243+37G= ENSP00000370839.5:n.243+37G=
ENST00000506357.5:c.229+37G=
ENST00000514133.1:c.210+37G= ENSP00000425818.1:n.210+37G=
NM_000232.4:c.243+37G= , LRG_204t1:c.243+37G= NP_000223.1:n.243+37G=
XM_006714049.2:c.-165+37G= XP_006714112.1:n.-165+37G=
XM_011534403.1:c.34-3531G= XP_011532705.1:n.34-3531G=
XM_011534404.1:c.-142+37G= XP_011532706.1:n.-142+37G=
NM_000232.5:c.243+37G= MANE Select NP_000223.1:n.243+37G=