Canonical Allele Identifier: CA356876283
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.632A>C MANE Select ENSP00000370839.6:p.Asn211Thr
ENST00000381431.9:c.632A>C ENSP00000370839.5:p.Asn211Thr
NM_000232.4:c.632A>C , LRG_204t1:c.632A>C NP_000223.1:p.Asn211Thr
XM_006714049.2:c.335A>C XP_006714112.1:p.Asn112Thr
XM_011534403.1:c.422A>C XP_011532705.1:p.Asn141Thr
XM_011534404.1:c.335A>C XP_011532706.1:p.Asn112Thr
NM_000232.5:c.632A>C MANE Select NP_000223.1:p.Asn211Thr