Canonical Allele Identifier: CA3114731

Gene: FGB

Linked Data

• dbSNP Id: rs765976401
• ExAC: 4:155490859 G / T
• gnomAD v2: 4-155490859-G-T
• gnomAD v4: 4-154569707-G-T
• MyVariant Identifiers: chr4:g.155490859G>T (hg19) ; chr4:g.154569707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569707G>T , CM000666.2:g.154569707G>T	GRCh38
NC_000004.11:g.155490859G>T , CM000666.1:g.155490859G>T	GRCh37
NC_000004.10:g.155710309G>T	NCBI36
NG_008833.1:g.11728G>T , LRG_558:g.11728G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.1152G>T MANE Select	ENSP00000306099.4:p.Met384Ile
ENST00000302068.8:c.1152G>T	ENSP00000306099.4:p.Met384Ile
ENST00000502545.5:n.939+400G>T
ENST00000509493.1:c.495G>T	ENSP00000426757.1:p.Met165Ile
NM_001184741.1:c.975G>T	NP_001171670.1:p.Met325Ile
NM_005141.4:c.1152G>T , LRG_558t1:c.1152G>T	NP_005132.2:p.Met384Ile
NM_001382759.1:c.1020G>T	NP_001369688.1:p.Met340Ile
NM_001382760.1:c.1152G>T	NP_001369689.1:p.Met384Ile
NM_001382761.1:c.1152G>T	NP_001369690.1:p.Met384Ile
NM_001382762.1:c.852G>T	NP_001369691.1:p.Met284Ile
NM_001382763.1:c.1143G>T	NP_001369692.1:p.Met381Ile
NM_001382764.1:c.1081-66G>T	NP_001369693.1:n.1081-66G>T
NM_001382765.1:c.1152G>T	NP_001369694.1:p.Met384Ile
NM_005141.5:c.1152G>T MANE Select	NP_005132.2:p.Met384Ile