Canonical Allele Identifier: CA108751924

Gene: FGB

Linked Data

• dbSNP Id: rs562205548
• gnomAD v2: 4-155491228-T-C
• gnomAD v3: 4-154570076-T-C
• gnomAD v4: 4-154570076-T-C
• MyVariant Identifiers: chr4:g.155491228T>C (hg19) ; chr4:g.154570076T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154570076T>C , CM000666.2:g.154570076T>C	GRCh38
NC_000004.11:g.155491228T>C , CM000666.1:g.155491228T>C	GRCh37
NC_000004.10:g.155710678T>C	NCBI36
NG_008833.1:g.12097T>C , LRG_558:g.12097T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244+277T>C MANE Select	ENSP00000306099.4:n.1244+277T>C
ENST00000302068.8:c.1244+277T>C	ENSP00000306099.4:n.1244+277T>C
ENST00000502545.5:n.940-343T>C
ENST00000509493.1:c.587+277T>C	ENSP00000426757.1:n.587+277T>C
NM_001184741.1:c.1067+277T>C	NP_001171670.1:n.1067+277T>C
NM_005141.4:c.1244+277T>C , LRG_558t1:c.1244+277T>C	NP_005132.2:n.1244+277T>C
NM_001382759.1:c.1112+277T>C	NP_001369688.1:n.1112+277T>C
NM_001382760.1:c.1244+277T>C	NP_001369689.1:n.1244+277T>C
NM_001382761.1:c.1244+277T>C	NP_001369690.1:n.1244+277T>C
NM_001382762.1:c.944+277T>C	NP_001369691.1:n.944+277T>C
NM_001382763.1:c.1235+277T>C	NP_001369692.1:n.1235+277T>C
NM_001382764.1:c.*18+277T>C	NP_001369693.1:n.*18+277T>C
NM_001382765.1:c.1220+301T>C	NP_001369694.1:n.1220+301T>C
NM_005141.5:c.1244+277T>C MANE Select	NP_005132.2:n.1244+277T>C