Canonical Allele Identifier: CA1457429168
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028089T= , CM000666.2:g.52028089T= GRCh38
NC_000004.11:g.52894255T= , CM000666.1:g.52894255T= GRCh37
NC_000004.10:g.52589012T= NCBI36
NG_008891.1:g.15231A= , LRG_204:g.15231A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.632A= MANE Select ENSP00000370839.6:p.Asn211=
ENST00000381431.9:c.632A= ENSP00000370839.5:p.Asn211=
NM_000232.4:c.632A= , LRG_204t1:c.632A= NP_000223.1:p.Asn211=
XM_006714049.2:c.335A= XP_006714112.1:p.Asn112=
XM_011534403.1:c.422A= XP_011532705.1:p.Asn141=
XM_011534404.1:c.335A= XP_011532706.1:p.Asn112=
NM_000232.5:c.632A= MANE Select NP_000223.1:p.Asn211=