Canonical Allele Identifier: CA356878046

Gene: SGCB

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.116A>G MANE Select	ENSP00000370839.6:p.Asn39Ser
ENST00000381431.9:c.116A>G	ENSP00000370839.5:p.Asn39Ser
ENST00000506357.5:c.102A>G
ENST00000514133.1:c.83A>G	ENSP00000425818.1:p.Asn28Ser
NM_000232.4:c.116A>G , LRG_204t1:c.116A>G	NP_000223.1:p.Asn39Ser
XM_011534403.1:c.34-3695A>G	XP_011532705.1:n.34-3695A>G
NM_000232.5:c.116A>G MANE Select	NP_000223.1:p.Asn39Ser