Canonical Allele Identifier: CA356876277
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028088A>C , CM000666.2:g.52028088A>C GRCh38
NC_000004.11:g.52894254A>C , CM000666.1:g.52894254A>C GRCh37
NC_000004.10:g.52589011A>C NCBI36
NG_008891.1:g.15232T>G , LRG_204:g.15232T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.633T>G MANE Select ENSP00000370839.6:p.Asn211Lys
ENST00000381431.9:c.633T>G ENSP00000370839.5:p.Asn211Lys
NM_000232.4:c.633T>G , LRG_204t1:c.633T>G NP_000223.1:p.Asn211Lys
XM_006714049.2:c.336T>G XP_006714112.1:p.Asn112Lys
XM_011534403.1:c.423T>G XP_011532705.1:p.Asn141Lys
XM_011534404.1:c.336T>G XP_011532706.1:p.Asn112Lys
NM_000232.5:c.633T>G MANE Select NP_000223.1:p.Asn211Lys