Canonical Allele Identifier: CA1457431741
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033505A= , CM000666.2:g.52033505A= GRCh38
NC_000004.11:g.52899671A= , CM000666.1:g.52899671A= GRCh37
NC_000004.10:g.52594428A= NCBI36
NG_008891.1:g.9815T= , LRG_204:g.9815T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.169T= MANE Select ENSP00000370839.6:p.Leu57=
ENST00000381431.9:c.169T= ENSP00000370839.5:p.Leu57=
ENST00000506357.5:c.155T=
ENST00000514133.1:c.136T= ENSP00000425818.1:p.Leu46=
NM_000232.4:c.169T= , LRG_204t1:c.169T= NP_000223.1:p.Leu57=
XM_006714049.2:c.-239T= XP_006714112.1:n.-239T=
XM_011534403.1:c.34-3642T= XP_011532705.1:n.34-3642T=
XM_011534404.1:c.-216T= XP_011532706.1:n.-216T=
NM_000232.5:c.169T= MANE Select NP_000223.1:p.Leu57=