Canonical Allele Identifier: CA358514598

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569529G>C , CM000666.2:g.154569529G>C	GRCh38
NC_000004.11:g.155490681G>C , CM000666.1:g.155490681G>C	GRCh37
NC_000004.10:g.155710131G>C	NCBI36
NG_008833.1:g.11550G>C , LRG_558:g.11550G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005141.5:c.974G>C MANE Select	NP_005132.2:p.Gly325Ala
ENST00000302068.9:c.974G>C MANE Select	ENSP00000306099.4:p.Gly325Ala
NM_001184741.1:c.797G>C	NP_001171670.1:p.Gly266Ala
NM_001382759.1:c.842G>C	NP_001369688.1:p.Gly281Ala
NM_001382760.1:c.974G>C	NP_001369689.1:p.Gly325Ala
NM_001382761.1:c.974G>C	NP_001369690.1:p.Gly325Ala
NM_001382762.1:c.746-72G>C	NP_001369691.1:n.746-72G>C
NM_001382763.1:c.965G>C	NP_001369692.1:p.Gly322Ala
NM_001382764.1:c.974G>C	NP_001369693.1:p.Gly325Ala
NM_001382765.1:c.974G>C	NP_001369694.1:p.Gly325Ala
NM_005141.4:c.974G>C , LRG_558t1:c.974G>C	NP_005132.2:p.Gly325Ala
ENST00000302068.8:c.974G>C	ENSP00000306099.4:p.Gly325Ala
ENST00000502545.5:n.939+222G>C
ENST00000509493.1:c.317G>C	ENSP00000426757.1:p.Gly106Ala