Canonical Allele Identifier: CA442013574

Gene: FGB

Linked Data

• dbSNP Id: rs1398387017
• gnomAD v2: 4-155490895-C-G
• gnomAD v4: 4-154569743-C-G
• MyVariant Identifiers: chr4:g.155490895C>G (hg19) ; chr4:g.154569743C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569743C>G , CM000666.2:g.154569743C>G	GRCh38
NC_000004.11:g.155490895C>G , CM000666.1:g.155490895C>G	GRCh37
NC_000004.10:g.155710345C>G	NCBI36
NG_008833.1:g.11764C>G , LRG_558:g.11764C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1188C>G MANE Select	ENSP00000306099.4:p.Thr396=
ENST00000302068.8:c.1188C>G	ENSP00000306099.4:p.Thr396=
ENST00000502545.5:n.939+436C>G
ENST00000509493.1:c.531C>G	ENSP00000426757.1:p.Thr177=
NM_001184741.1:c.1011C>G	NP_001171670.1:p.Thr337=
NM_005141.4:c.1188C>G , LRG_558t1:c.1188C>G	NP_005132.2:p.Thr396=
NM_001382759.1:c.1056C>G	NP_001369688.1:p.Thr352=
NM_001382760.1:c.1188C>G	NP_001369689.1:p.Thr396=
NM_001382761.1:c.1188C>G	NP_001369690.1:p.Thr396=
NM_001382762.1:c.888C>G	NP_001369691.1:p.Thr296=
NM_001382763.1:c.1179C>G	NP_001369692.1:p.Thr393=
NM_001382764.1:c.1081-30C>G	NP_001369693.1:n.1081-30C>G
NM_001382765.1:c.1188C>G	NP_001369694.1:p.Thr396=
NM_005141.5:c.1188C>G MANE Select	NP_005132.2:p.Thr396=