Canonical Allele Identifier: CA441809381

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155487016C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565864C>G , CM000666.2:g.154565864C>G	GRCh38
NC_000004.11:g.155487016C>G , CM000666.1:g.155487016C>G	GRCh37
NC_000004.10:g.155706466C>G	NCBI36
NG_008833.1:g.7885C>G , LRG_558:g.7885C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.171C>G MANE Select	ENSP00000306099.4:p.Pro57=
ENST00000302068.8:c.171C>G	ENSP00000306099.4:p.Pro57=
ENST00000425838.5:c.*83C>G	ENSP00000398719.1:n.*83C>G
ENST00000473984.1:n.84C>G
ENST00000497097.5:n.178C>G
ENST00000498375.2:n.801C>G
ENST00000502545.5:n.152C>G
ENST00000509493.1:c.-167-1729C>G	ENSP00000426757.1:n.-167-1729C>G
NM_001184741.1:c.165+6C>G	NP_001171670.1:n.165+6C>G
NM_005141.4:c.171C>G , LRG_558t1:c.171C>G	NP_005132.2:p.Pro57=
NM_001382759.1:c.171C>G	NP_001369688.1:p.Pro57=
NM_001382760.1:c.171C>G	NP_001369689.1:p.Pro57=
NM_001382761.1:c.171C>G	NP_001369690.1:p.Pro57=
NM_001382762.1:c.171C>G	NP_001369691.1:p.Pro57=
NM_001382763.1:c.171C>G	NP_001369692.1:p.Pro57=
NM_001382764.1:c.171C>G	NP_001369693.1:p.Pro57=
NM_001382765.1:c.171C>G	NP_001369694.1:p.Pro57=
NM_005141.5:c.171C>G MANE Select	NP_005132.2:p.Pro57=