Canonical Allele Identifier: CA356878127
Gene: SGCB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.52899758C>T (hg19) chr4:g.52033592C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033592C>T , CM000666.2:g.52033592C>T GRCh38
NC_000004.11:g.52899758C>T , CM000666.1:g.52899758C>T GRCh37
NC_000004.10:g.52594515C>T NCBI36
NG_008891.1:g.9728G>A , LRG_204:g.9728G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.82G>A MANE Select ENSP00000370839.6:p.Glu28Lys
ENST00000381431.9:c.82G>A ENSP00000370839.5:p.Glu28Lys
ENST00000506357.5:c.68G>A
ENST00000514133.1:c.49G>A ENSP00000425818.1:p.Glu17Lys
NM_000232.4:c.82G>A , LRG_204t1:c.82G>A NP_000223.1:p.Glu28Lys
XM_011534403.1:c.34-3729G>A XP_011532705.1:n.34-3729G>A
NM_000232.5:c.82G>A MANE Select NP_000223.1:p.Glu28Lys
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