Canonical Allele Identifier: CA358515444

Gene: FGB

Linked Data

• gnomAD v4: 4-154569746-G-C
• MyVariant Identifiers: chr4:g.155490898G>C (hg19) ; chr4:g.154569746G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569746G>C , CM000666.2:g.154569746G>C	GRCh38
NC_000004.11:g.155490898G>C , CM000666.1:g.155490898G>C	GRCh37
NC_000004.10:g.155710348G>C	NCBI36
NG_008833.1:g.11767G>C , LRG_558:g.11767G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1191G>C MANE Select	ENSP00000306099.4:p.Met397Ile
ENST00000302068.8:c.1191G>C	ENSP00000306099.4:p.Met397Ile
ENST00000502545.5:n.939+439G>C
ENST00000509493.1:c.534G>C	ENSP00000426757.1:p.Met178Ile
NM_001184741.1:c.1014G>C	NP_001171670.1:p.Met338Ile
NM_005141.4:c.1191G>C , LRG_558t1:c.1191G>C	NP_005132.2:p.Met397Ile
NM_001382759.1:c.1059G>C	NP_001369688.1:p.Met353Ile
NM_001382760.1:c.1191G>C	NP_001369689.1:p.Met397Ile
NM_001382761.1:c.1191G>C	NP_001369690.1:p.Met397Ile
NM_001382762.1:c.891G>C	NP_001369691.1:p.Met297Ile
NM_001382763.1:c.1182G>C	NP_001369692.1:p.Met394Ile
NM_001382764.1:c.1081-27G>C	NP_001369693.1:n.1081-27G>C
NM_001382765.1:c.1191G>C	NP_001369694.1:p.Met397Ile
NM_005141.5:c.1191G>C MANE Select	NP_005132.2:p.Met397Ile