Canonical Allele Identifier: CA1457429141
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028026A= , CM000666.2:g.52028026A= GRCh38
NC_000004.11:g.52894192A= , CM000666.1:g.52894192A= GRCh37
NC_000004.10:g.52588949A= NCBI36
NG_008891.1:g.15294T= , LRG_204:g.15294T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.695T= MANE Select ENSP00000370839.6:p.Val232=
ENST00000381431.9:c.695T= ENSP00000370839.5:p.Val232=
NM_000232.4:c.695T= , LRG_204t1:c.695T= NP_000223.1:p.Val232=
XM_006714049.2:c.398T= XP_006714112.1:p.Val133=
XM_011534403.1:c.485T= XP_011532705.1:p.Val162=
XM_011534404.1:c.398T= XP_011532706.1:p.Val133=
NM_000232.5:c.695T= MANE Select NP_000223.1:p.Val232=