Canonical Allele Identifier: CA1457429115
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027971C= , CM000666.2:g.52027971C= GRCh38
NC_000004.11:g.52894137C= , CM000666.1:g.52894137C= GRCh37
NC_000004.10:g.52588894C= NCBI36
NG_008891.1:g.15349G= , LRG_204:g.15349G=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.750G= MANE Select ENSP00000370839.6:p.Lys250=
ENST00000381431.9:c.750G= ENSP00000370839.5:p.Lys250=
NM_000232.4:c.750G= , LRG_204t1:c.750G= NP_000223.1:p.Lys250=
XM_006714049.2:c.453G= XP_006714112.1:p.Lys151=
XM_011534403.1:c.540G= XP_011532705.1:p.Lys180=
XM_011534404.1:c.453G= XP_011532706.1:p.Lys151=
NM_000232.5:c.750G= MANE Select NP_000223.1:p.Lys250=