Canonical Allele Identifier: CA1457429137
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028021T= , CM000666.2:g.52028021T= GRCh38
NC_000004.11:g.52894187T= , CM000666.1:g.52894187T= GRCh37
NC_000004.10:g.52588944T= NCBI36
NG_008891.1:g.15299A= , LRG_204:g.15299A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.700A= MANE Select ENSP00000370839.6:p.Ile234=
ENST00000381431.9:c.700A= ENSP00000370839.5:p.Ile234=
NM_000232.4:c.700A= , LRG_204t1:c.700A= NP_000223.1:p.Ile234=
XM_006714049.2:c.403A= XP_006714112.1:p.Ile135=
XM_011534403.1:c.490A= XP_011532705.1:p.Ile164=
XM_011534404.1:c.403A= XP_011532706.1:p.Ile135=
NM_000232.5:c.700A= MANE Select NP_000223.1:p.Ile234=