Canonical Allele Identifier: CA1457431761
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033542G= , CM000666.2:g.52033542G= GRCh38
NC_000004.11:g.52899708G= , CM000666.1:g.52899708G= GRCh37
NC_000004.10:g.52594465G= NCBI36
NG_008891.1:g.9778C= , LRG_204:g.9778C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.132C= MANE Select ENSP00000370839.6:p.Tyr44=
ENST00000381431.9:c.132C= ENSP00000370839.5:p.Tyr44=
ENST00000506357.5:c.118C=
ENST00000514133.1:c.99C= ENSP00000425818.1:p.Tyr33=
NM_000232.4:c.132C= , LRG_204t1:c.132C= NP_000223.1:p.Tyr44=
XM_011534403.1:c.34-3679C= XP_011532705.1:n.34-3679C=
NM_000232.5:c.132C= MANE Select NP_000223.1:p.Tyr44=