Canonical Allele Identifier: CA356878047

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52899724T>G (hg19) ; chr4:g.52033558T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52033558T>G , CM000666.2:g.52033558T>G	GRCh38
NC_000004.11:g.52899724T>G , CM000666.1:g.52899724T>G	GRCh37
NC_000004.10:g.52594481T>G	NCBI36
NG_008891.1:g.9762A>C , LRG_204:g.9762A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.116A>C MANE Select	ENSP00000370839.6:p.Asn39Thr
ENST00000381431.9:c.116A>C	ENSP00000370839.5:p.Asn39Thr
ENST00000506357.5:c.102A>C
ENST00000514133.1:c.83A>C	ENSP00000425818.1:p.Asn28Thr
NM_000232.4:c.116A>C , LRG_204t1:c.116A>C	NP_000223.1:p.Asn39Thr
XM_011534403.1:c.34-3695A>C	XP_011532705.1:n.34-3695A>C
NM_000232.5:c.116A>C MANE Select	NP_000223.1:p.Asn39Thr