Canonical Allele Identifier: CA555971634

Gene: FGB

Linked Data

• dbSNP Id: rs1391344093
• gnomAD v2: 4-155490955-T-A
• gnomAD v3: 4-154569803-T-A
• gnomAD v4: 4-154569803-T-A
• MyVariant Identifiers: chr4:g.155490955T>A (hg19) ; chr4:g.154569803T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569803T>A , CM000666.2:g.154569803T>A	GRCh38
NC_000004.11:g.155490955T>A , CM000666.1:g.155490955T>A	GRCh37
NC_000004.10:g.155710405T>A	NCBI36
NG_008833.1:g.11824T>A , LRG_558:g.11824T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244+4T>A MANE Select	ENSP00000306099.4:n.1244+4T>A
ENST00000302068.8:c.1244+4T>A	ENSP00000306099.4:n.1244+4T>A
ENST00000502545.5:n.939+496T>A
ENST00000509493.1:c.587+4T>A	ENSP00000426757.1:n.587+4T>A
NM_001184741.1:c.1067+4T>A	NP_001171670.1:n.1067+4T>A
NM_005141.4:c.1244+4T>A , LRG_558t1:c.1244+4T>A	NP_005132.2:n.1244+4T>A
NM_001382759.1:c.1112+4T>A	NP_001369688.1:n.1112+4T>A
NM_001382760.1:c.1244+4T>A	NP_001369689.1:n.1244+4T>A
NM_001382761.1:c.1244+4T>A	NP_001369690.1:n.1244+4T>A
NM_001382762.1:c.944+4T>A	NP_001369691.1:n.944+4T>A
NM_001382763.1:c.1235+4T>A	NP_001369692.1:n.1235+4T>A
NM_001382764.1:c.*18+4T>A	NP_001369693.1:n.*18+4T>A
NM_001382765.1:c.1220+28T>A	NP_001369694.1:n.1220+28T>A
NM_005141.5:c.1244+4T>A MANE Select	NP_005132.2:n.1244+4T>A