Canonical Allele Identifier: CA2918321
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs550062936
gnomAD v2: 4-52894208-G-A
gnomAD v3: 4-52028042-G-A
gnomAD v4: 4-52028042-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028042G>A , CM000666.2:g.52028042G>A GRCh38
NC_000004.11:g.52894208G>A , CM000666.1:g.52894208G>A GRCh37
NC_000004.10:g.52588965G>A NCBI36
NG_008891.1:g.15278C>T , LRG_204:g.15278C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.679C>T MANE Select ENSP00000370839.6:p.Arg227Cys
ENST00000381431.9:c.679C>T ENSP00000370839.5:p.Arg227Cys
NM_000232.4:c.679C>T , LRG_204t1:c.679C>T NP_000223.1:p.Arg227Cys
XM_006714049.2:c.382C>T XP_006714112.1:p.Arg128Cys
XM_011534403.1:c.469C>T XP_011532705.1:p.Arg157Cys
XM_011534404.1:c.382C>T XP_011532706.1:p.Arg128Cys
NM_000232.5:c.679C>T MANE Select NP_000223.1:p.Arg227Cys