Canonical Allele Identifier: CA1457431734
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033470C= , CM000666.2:g.52033470C= GRCh38
NC_000004.11:g.52899636C= , CM000666.1:g.52899636C= GRCh37
NC_000004.10:g.52594393C= NCBI36
NG_008891.1:g.9850G= , LRG_204:g.9850G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.204G= MANE Select ENSP00000370839.6:p.Val68=
ENST00000381431.9:c.204G= ENSP00000370839.5:p.Val68=
ENST00000506357.5:c.190G=
ENST00000514133.1:c.171G= ENSP00000425818.1:p.Val57=
NM_000232.4:c.204G= , LRG_204t1:c.204G= NP_000223.1:p.Val68=
XM_006714049.2:c.-204G= XP_006714112.1:n.-204G=
XM_011534403.1:c.34-3607G= XP_011532705.1:n.34-3607G=
XM_011534404.1:c.-181G= XP_011532706.1:n.-181G=
NM_000232.5:c.204G= MANE Select NP_000223.1:p.Val68=