Canonical Allele Identifier: CA356876049
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52028041-C-A
COSMIC: COSM734219

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028041C>A , CM000666.2:g.52028041C>A GRCh38
NC_000004.11:g.52894207C>A , CM000666.1:g.52894207C>A GRCh37
NC_000004.10:g.52588964C>A NCBI36
NG_008891.1:g.15279G>T , LRG_204:g.15279G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.680G>T MANE Select ENSP00000370839.6:p.Arg227Leu
ENST00000381431.9:c.680G>T ENSP00000370839.5:p.Arg227Leu
NM_000232.4:c.680G>T , LRG_204t1:c.680G>T NP_000223.1:p.Arg227Leu
XM_006714049.2:c.383G>T XP_006714112.1:p.Arg128Leu
XM_011534403.1:c.470G>T XP_011532705.1:p.Arg157Leu
XM_011534404.1:c.383G>T XP_011532706.1:p.Arg128Leu
NM_000232.5:c.680G>T MANE Select NP_000223.1:p.Arg227Leu