Canonical Allele Identifier: CA356878125

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52899757T>A (hg19) ; chr4:g.52033591T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52033591T>A , CM000666.2:g.52033591T>A	GRCh38
NC_000004.11:g.52899757T>A , CM000666.1:g.52899757T>A	GRCh37
NC_000004.10:g.52594514T>A	NCBI36
NG_008891.1:g.9729A>T , LRG_204:g.9729A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.83A>T MANE Select	ENSP00000370839.6:p.Glu28Val
ENST00000381431.9:c.83A>T	ENSP00000370839.5:p.Glu28Val
ENST00000506357.5:c.69A>T
ENST00000514133.1:c.50A>T	ENSP00000425818.1:p.Glu17Val
NM_000232.4:c.83A>T , LRG_204t1:c.83A>T	NP_000223.1:p.Glu28Val
XM_011534403.1:c.34-3728A>T	XP_011532705.1:n.34-3728A>T
NM_000232.5:c.83A>T MANE Select	NP_000223.1:p.Glu28Val