Canonical Allele Identifier: CA358515291

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490857A>C (hg19) ; chr4:g.154569705A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569705A>C , CM000666.2:g.154569705A>C	GRCh38
NC_000004.11:g.155490857A>C , CM000666.1:g.155490857A>C	GRCh37
NC_000004.10:g.155710307A>C	NCBI36
NG_008833.1:g.11726A>C , LRG_558:g.11726A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1150A>C MANE Select	ENSP00000306099.4:p.Met384Leu
ENST00000302068.8:c.1150A>C	ENSP00000306099.4:p.Met384Leu
ENST00000502545.5:n.939+398A>C
ENST00000509493.1:c.493A>C	ENSP00000426757.1:p.Met165Leu
NM_001184741.1:c.973A>C	NP_001171670.1:p.Met325Leu
NM_005141.4:c.1150A>C , LRG_558t1:c.1150A>C	NP_005132.2:p.Met384Leu
NM_001382759.1:c.1018A>C	NP_001369688.1:p.Met340Leu
NM_001382760.1:c.1150A>C	NP_001369689.1:p.Met384Leu
NM_001382761.1:c.1150A>C	NP_001369690.1:p.Met384Leu
NM_001382762.1:c.850A>C	NP_001369691.1:p.Met284Leu
NM_001382763.1:c.1141A>C	NP_001369692.1:p.Met381Leu
NM_001382764.1:c.1081-68A>C	NP_001369693.1:n.1081-68A>C
NM_001382765.1:c.1150A>C	NP_001369694.1:p.Met384Leu
NM_005141.5:c.1150A>C MANE Select	NP_005132.2:p.Met384Leu