Canonical Allele Identifier: CA358515622

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490941A>G (hg19) ; chr4:g.154569789A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569789A>G , CM000666.2:g.154569789A>G	GRCh38
NC_000004.11:g.155490941A>G , CM000666.1:g.155490941A>G	GRCh37
NC_000004.10:g.155710391A>G	NCBI36
NG_008833.1:g.11810A>G , LRG_558:g.11810A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1234A>G MANE Select	ENSP00000306099.4:p.Asn412Asp
ENST00000302068.8:c.1234A>G	ENSP00000306099.4:p.Asn412Asp
ENST00000502545.5:n.939+482A>G
ENST00000509493.1:c.577A>G	ENSP00000426757.1:p.Asn193Asp
NM_001184741.1:c.1057A>G	NP_001171670.1:p.Asn353Asp
NM_005141.4:c.1234A>G , LRG_558t1:c.1234A>G	NP_005132.2:p.Asn412Asp
NM_001382759.1:c.1102A>G	NP_001369688.1:p.Asn368Asp
NM_001382760.1:c.1234A>G	NP_001369689.1:p.Asn412Asp
NM_001382761.1:c.1234A>G	NP_001369690.1:p.Asn412Asp
NM_001382762.1:c.934A>G	NP_001369691.1:p.Asn312Asp
NM_001382763.1:c.1225A>G	NP_001369692.1:p.Asn409Asp
NM_001382764.1:c.*8A>G	NP_001369693.1:n.*8A>G
NM_001382765.1:c.1220+14A>G	NP_001369694.1:n.1220+14A>G
NM_005141.5:c.1234A>G MANE Select	NP_005132.2:p.Asn412Asp