Canonical Allele Identifier: CA358515600

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490936G>C (hg19) ; chr4:g.154569784G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569784G>C , CM000666.2:g.154569784G>C	GRCh38
NC_000004.11:g.155490936G>C , CM000666.1:g.155490936G>C	GRCh37
NC_000004.10:g.155710386G>C	NCBI36
NG_008833.1:g.11805G>C , LRG_558:g.11805G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1229G>C MANE Select	ENSP00000306099.4:p.Arg410Thr
ENST00000302068.8:c.1229G>C	ENSP00000306099.4:p.Arg410Thr
ENST00000502545.5:n.939+477G>C
ENST00000509493.1:c.572G>C	ENSP00000426757.1:p.Arg191Thr
NM_001184741.1:c.1052G>C	NP_001171670.1:p.Arg351Thr
NM_005141.4:c.1229G>C , LRG_558t1:c.1229G>C	NP_005132.2:p.Arg410Thr
NM_001382759.1:c.1097G>C	NP_001369688.1:p.Arg366Thr
NM_001382760.1:c.1229G>C	NP_001369689.1:p.Arg410Thr
NM_001382761.1:c.1229G>C	NP_001369690.1:p.Arg410Thr
NM_001382762.1:c.929G>C	NP_001369691.1:p.Arg310Thr
NM_001382763.1:c.1220G>C	NP_001369692.1:p.Arg407Thr
NM_001382764.1:c.*3G>C	NP_001369693.1:n.*3G>C
NM_001382765.1:c.1220+9G>C	NP_001369694.1:n.1220+9G>C
NM_005141.5:c.1229G>C MANE Select	NP_005132.2:p.Arg410Thr