Canonical Allele Identifier: CA439274736

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52899663T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52033497T>A , CM000666.2:g.52033497T>A	GRCh38
NC_000004.11:g.52899663T>A , CM000666.1:g.52899663T>A	GRCh37
NC_000004.10:g.52594420T>A	NCBI36
NG_008891.1:g.9823A>T , LRG_204:g.9823A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.177A>T MANE Select	ENSP00000370839.6:p.Gly59=
ENST00000381431.9:c.177A>T	ENSP00000370839.5:p.Gly59=
ENST00000506357.5:c.163A>T
ENST00000514133.1:c.144A>T	ENSP00000425818.1:p.Gly48=
NM_000232.4:c.177A>T , LRG_204t1:c.177A>T	NP_000223.1:p.Gly59=
XM_006714049.2:c.-231A>T	XP_006714112.1:n.-231A>T
XM_011534403.1:c.34-3634A>T	XP_011532705.1:n.34-3634A>T
XM_011534404.1:c.-208A>T	XP_011532706.1:n.-208A>T
NM_000232.5:c.177A>T MANE Select	NP_000223.1:p.Gly59=