Canonical Allele Identifier: CA356876016
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028033C>G , CM000666.2:g.52028033C>G GRCh38
NC_000004.11:g.52894199C>G , CM000666.1:g.52894199C>G GRCh37
NC_000004.10:g.52588956C>G NCBI36
NG_008891.1:g.15287G>C , LRG_204:g.15287G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.688G>C MANE Select ENSP00000370839.6:p.Glu230Gln
ENST00000381431.9:c.688G>C ENSP00000370839.5:p.Glu230Gln
NM_000232.4:c.688G>C , LRG_204t1:c.688G>C NP_000223.1:p.Glu230Gln
XM_006714049.2:c.391G>C XP_006714112.1:p.Glu131Gln
XM_011534403.1:c.478G>C XP_011532705.1:p.Glu160Gln
XM_011534404.1:c.391G>C XP_011532706.1:p.Glu131Gln
NM_000232.5:c.688G>C MANE Select NP_000223.1:p.Glu230Gln