Canonical Allele Identifier: CA356876121

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52894222C>T (hg19) ; chr4:g.52028056C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028056C>T , CM000666.2:g.52028056C>T	GRCh38
NC_000004.11:g.52894222C>T , CM000666.1:g.52894222C>T	GRCh37
NC_000004.10:g.52588979C>T	NCBI36
NG_008891.1:g.15264G>A , LRG_204:g.15264G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.665G>A MANE Select	ENSP00000370839.6:p.Gly222Glu
ENST00000381431.9:c.665G>A	ENSP00000370839.5:p.Gly222Glu
NM_000232.4:c.665G>A , LRG_204t1:c.665G>A	NP_000223.1:p.Gly222Glu
XM_006714049.2:c.368G>A	XP_006714112.1:p.Gly123Glu
XM_011534403.1:c.455G>A	XP_011532705.1:p.Gly152Glu
XM_011534404.1:c.368G>A	XP_011532706.1:p.Gly123Glu
NM_000232.5:c.665G>A MANE Select	NP_000223.1:p.Gly222Glu