Canonical Allele Identifier: CA1457431784
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033593A= , CM000666.2:g.52033593A= GRCh38
NC_000004.11:g.52899759A= , CM000666.1:g.52899759A= GRCh37
NC_000004.10:g.52594516A= NCBI36
NG_008891.1:g.9727T= , LRG_204:g.9727T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.81T= MANE Select ENSP00000370839.6:p.Val27=
ENST00000381431.9:c.81T= ENSP00000370839.5:p.Val27=
ENST00000506357.5:c.67T=
ENST00000514133.1:c.48T= ENSP00000425818.1:p.Val16=
NM_000232.4:c.81T= , LRG_204t1:c.81T= NP_000223.1:p.Val27=
XM_011534403.1:c.34-3730T= XP_011532705.1:n.34-3730T=
NM_000232.5:c.81T= MANE Select NP_000223.1:p.Val27=