Canonical Allele Identifier: CA358515119

Gene: FGB

Linked Data

• gnomAD v4: 4-154569657-T-C
• MyVariant Identifiers: chr4:g.155490809T>C (hg19) ; chr4:g.154569657T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569657T>C , CM000666.2:g.154569657T>C	GRCh38
NC_000004.11:g.155490809T>C , CM000666.1:g.155490809T>C	GRCh37
NC_000004.10:g.155710259T>C	NCBI36
NG_008833.1:g.11678T>C , LRG_558:g.11678T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1102T>C MANE Select	ENSP00000306099.4:p.Tyr368His
ENST00000302068.8:c.1102T>C	ENSP00000306099.4:p.Tyr368His
ENST00000502545.5:n.939+350T>C
ENST00000509493.1:c.445T>C	ENSP00000426757.1:p.Tyr149His
NM_001184741.1:c.925T>C	NP_001171670.1:p.Tyr309His
NM_005141.4:c.1102T>C , LRG_558t1:c.1102T>C	NP_005132.2:p.Tyr368His
NM_001382759.1:c.970T>C	NP_001369688.1:p.Tyr324His
NM_001382760.1:c.1102T>C	NP_001369689.1:p.Tyr368His
NM_001382761.1:c.1102T>C	NP_001369690.1:p.Tyr368His
NM_001382762.1:c.802T>C	NP_001369691.1:p.Tyr268His
NM_001382763.1:c.1093T>C	NP_001369692.1:p.Tyr365His
NM_001382764.1:c.1080+22T>C	NP_001369693.1:n.1080+22T>C
NM_001382765.1:c.1102T>C	NP_001369694.1:p.Tyr368His
NM_005141.5:c.1102T>C MANE Select	NP_005132.2:p.Tyr368His