Canonical Allele Identifier: CA356876090
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028050G>C , CM000666.2:g.52028050G>C GRCh38
NC_000004.11:g.52894216G>C , CM000666.1:g.52894216G>C GRCh37
NC_000004.10:g.52588973G>C NCBI36
NG_008891.1:g.15270C>G , LRG_204:g.15270C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.671C>G MANE Select ENSP00000370839.6:p.Ala224Gly
ENST00000381431.9:c.671C>G ENSP00000370839.5:p.Ala224Gly
NM_000232.4:c.671C>G , LRG_204t1:c.671C>G NP_000223.1:p.Ala224Gly
XM_006714049.2:c.374C>G XP_006714112.1:p.Ala125Gly
XM_011534403.1:c.461C>G XP_011532705.1:p.Ala154Gly
XM_011534404.1:c.374C>G XP_011532706.1:p.Ala125Gly
NM_000232.5:c.671C>G MANE Select NP_000223.1:p.Ala224Gly