Canonical Allele Identifier: CA358508882

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155487141A>C (hg19) ; chr4:g.154565989A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565989A>C , CM000666.2:g.154565989A>C	GRCh38
NC_000004.11:g.155487141A>C , CM000666.1:g.155487141A>C	GRCh37
NC_000004.10:g.155706591A>C	NCBI36
NG_008833.1:g.8010A>C , LRG_558:g.8010A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.296A>C MANE Select	ENSP00000306099.4:p.Asp99Ala
ENST00000302068.8:c.296A>C	ENSP00000306099.4:p.Asp99Ala
ENST00000425838.5:c.*208A>C	ENSP00000398719.1:n.*208A>C
ENST00000473984.1:n.209A>C
ENST00000497097.5:n.303A>C
ENST00000498375.2:n.926A>C
ENST00000502545.5:n.277A>C
ENST00000509493.1:c.-167-1604A>C	ENSP00000426757.1:n.-167-1604A>C
NM_001184741.1:c.165+131A>C	NP_001171670.1:n.165+131A>C
NM_005141.4:c.296A>C , LRG_558t1:c.296A>C	NP_005132.2:p.Asp99Ala
NM_001382759.1:c.296A>C	NP_001369688.1:p.Asp99Ala
NM_001382760.1:c.296A>C	NP_001369689.1:p.Asp99Ala
NM_001382761.1:c.296A>C	NP_001369690.1:p.Asp99Ala
NM_001382762.1:c.296A>C	NP_001369691.1:p.Asp99Ala
NM_001382763.1:c.296A>C	NP_001369692.1:p.Asp99Ala
NM_001382764.1:c.296A>C	NP_001369693.1:p.Asp99Ala
NM_001382765.1:c.296A>C	NP_001369694.1:p.Asp99Ala
NM_005141.5:c.296A>C MANE Select	NP_005132.2:p.Asp99Ala