Canonical Allele Identifier: CA358515298

Gene: FGB

Linked Data

• gnomAD v4: 4-154569706-T-C
• MyVariant Identifiers: chr4:g.155490858T>C (hg19) ; chr4:g.154569706T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569706T>C , CM000666.2:g.154569706T>C	GRCh38
NC_000004.11:g.155490858T>C , CM000666.1:g.155490858T>C	GRCh37
NC_000004.10:g.155710308T>C	NCBI36
NG_008833.1:g.11727T>C , LRG_558:g.11727T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.1151T>C MANE Select	ENSP00000306099.4:p.Met384Thr
ENST00000302068.8:c.1151T>C	ENSP00000306099.4:p.Met384Thr
ENST00000502545.5:n.939+399T>C
ENST00000509493.1:c.494T>C	ENSP00000426757.1:p.Met165Thr
NM_001184741.1:c.974T>C	NP_001171670.1:p.Met325Thr
NM_005141.4:c.1151T>C , LRG_558t1:c.1151T>C	NP_005132.2:p.Met384Thr
NM_001382759.1:c.1019T>C	NP_001369688.1:p.Met340Thr
NM_001382760.1:c.1151T>C	NP_001369689.1:p.Met384Thr
NM_001382761.1:c.1151T>C	NP_001369690.1:p.Met384Thr
NM_001382762.1:c.851T>C	NP_001369691.1:p.Met284Thr
NM_001382763.1:c.1142T>C	NP_001369692.1:p.Met381Thr
NM_001382764.1:c.1081-67T>C	NP_001369693.1:n.1081-67T>C
NM_001382765.1:c.1151T>C	NP_001369694.1:p.Met384Thr
NM_005141.5:c.1151T>C MANE Select	NP_005132.2:p.Met384Thr