Canonical Allele Identifier: CA358514975

Gene: FGB

Linked Data

• gnomAD v4: 4-154569620-C-G
• MyVariant Identifiers: chr4:g.155490772C>G (hg19) ; chr4:g.154569620C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569620C>G , CM000666.2:g.154569620C>G	GRCh38
NC_000004.11:g.155490772C>G , CM000666.1:g.155490772C>G	GRCh37
NC_000004.10:g.155710222C>G	NCBI36
NG_008833.1:g.11641C>G , LRG_558:g.11641C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1065C>G MANE Select	ENSP00000306099.4:p.His355Gln
ENST00000302068.8:c.1065C>G	ENSP00000306099.4:p.His355Gln
ENST00000502545.5:n.939+313C>G
ENST00000509493.1:c.408C>G	ENSP00000426757.1:p.His136Gln
NM_001184741.1:c.888C>G	NP_001171670.1:p.His296Gln
NM_005141.4:c.1065C>G , LRG_558t1:c.1065C>G	NP_005132.2:p.His355Gln
NM_001382759.1:c.933C>G	NP_001369688.1:p.His311Gln
NM_001382760.1:c.1065C>G	NP_001369689.1:p.His355Gln
NM_001382761.1:c.1065C>G	NP_001369690.1:p.His355Gln
NM_001382762.1:c.765C>G	NP_001369691.1:p.His255Gln
NM_001382763.1:c.1056C>G	NP_001369692.1:p.His352Gln
NM_001382764.1:c.1065C>G	NP_001369693.1:p.His355Gln
NM_001382765.1:c.1065C>G	NP_001369694.1:p.His355Gln
NM_005141.5:c.1065C>G MANE Select	NP_005132.2:p.His355Gln