Canonical Allele Identifier: CA356877365
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52029796T>G , CM000666.2:g.52029796T>G GRCh38
NC_000004.11:g.52895962T>G , CM000666.1:g.52895962T>G GRCh37
NC_000004.10:g.52590719T>G NCBI36
NG_008891.1:g.13524A>C , LRG_204:g.13524A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.311A>C MANE Select ENSP00000370839.6:p.Glu104Ala
ENST00000381431.9:c.311A>C ENSP00000370839.5:p.Glu104Ala
ENST00000506357.5:c.394A>C
ENST00000514133.1:c.388A>C ENSP00000425818.1:n.388A>C
NM_000232.4:c.311A>C , LRG_204t1:c.311A>C NP_000223.1:p.Glu104Ala
XM_006714049.2:c.14A>C XP_006714112.1:p.Glu5Ala
XM_011534403.1:c.101A>C XP_011532705.1:p.Glu34Ala
XM_011534404.1:c.14A>C XP_011532706.1:p.Glu5Ala
NM_000232.5:c.311A>C MANE Select NP_000223.1:p.Glu104Ala