Canonical Allele Identifier: CA356877322

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52895941T>G (hg19) ; chr4:g.52029775T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029775T>G , CM000666.2:g.52029775T>G	GRCh38
NC_000004.11:g.52895941T>G , CM000666.1:g.52895941T>G	GRCh37
NC_000004.10:g.52590698T>G	NCBI36
NG_008891.1:g.13545A>C , LRG_204:g.13545A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.332A>C MANE Select	ENSP00000370839.6:p.Lys111Thr
ENST00000381431.9:c.332A>C	ENSP00000370839.5:p.Lys111Thr
ENST00000506357.5:c.415A>C
ENST00000514133.1:c.409A>C	ENSP00000425818.1:n.409A>C
NM_000232.4:c.332A>C , LRG_204t1:c.332A>C	NP_000223.1:p.Lys111Thr
XM_006714049.2:c.35A>C	XP_006714112.1:p.Lys12Thr
XM_011534403.1:c.122A>C	XP_011532705.1:p.Lys41Thr
XM_011534404.1:c.35A>C	XP_011532706.1:p.Lys12Thr
NM_000232.5:c.332A>C MANE Select	NP_000223.1:p.Lys111Thr