Canonical Allele Identifier: CA10619269

Gene: FLNB

Linked Data

• ClinVar Variation Id: 346290
• ClinVar RCV Id: RCV000353683
• dbSNP Id: rs544100587
• gnomAD v2: 3-57994161-G-C
• gnomAD v3: 3-58008434-G-C
• gnomAD v4: 3-58008434-G-C
• MyVariant Identifiers: chr3:g.57994161G>C (hg19) ; chr3:g.58008434G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58008434G>C , CM000665.2:g.58008434G>C	GRCh38
NC_000003.11:g.57994161G>C , CM000665.1:g.57994161G>C	GRCh37
NC_000003.10:g.57969201G>C	NCBI36
NG_012801.1:g.5035G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682097.1:c.-131G>C	ENSP00000508183.1:n.-131G>C
ENST00000682868.1:n.13G>C
ENST00000682871.1:c.-131G>C	ENSP00000507805.1:n.-131G>C
ENST00000682987.1:n.13G>C
ENST00000683511.1:n.29G>C
ENST00000684107.1:c.-131G>C	ENSP00000507440.1:n.-131G>C
ENST00000684506.1:c.-131G>C	ENSP00000507728.1:n.-131G>C
ENST00000684517.1:c.-131G>C	ENSP00000507828.1:n.-131G>C
ENST00000684607.1:c.-131G>C	ENSP00000508224.1:n.-131G>C
ENST00000295956.9:c.-131G>C MANE Select	ENSP00000295956.5:n.-131G>C
ENST00000295956.8:c.-131G>C	ENSP00000295956.4:n.-131G>C
ENST00000358537.7:c.-131G>C	ENSP00000351339.3:n.-131G>C
ENST00000429972.6:c.-131G>C	ENSP00000415599.2:n.-131G>C
ENST00000490882.5:c.-131G>C	ENSP00000420213.1:n.-131G>C
NM_001164317.1:c.-131G>C	NP_001157789.1:n.-131G>C
NM_001164318.1:c.-131G>C	NP_001157790.1:n.-131G>C
NM_001164319.1:c.-131G>C	NP_001157791.1:n.-131G>C
NM_001457.3:c.-131G>C	NP_001448.2:n.-131G>C
XM_005264977.1:c.-131G>C	XP_005265034.1:n.-131G>C
XM_005264978.1:c.-131G>C	XP_005265035.1:n.-131G>C
XM_005264981.1:c.-131G>C	XP_005265038.1:n.-131G>C
XR_940396.1:n.15G>C
XM_005264978.2:c.-131G>C	XP_005265035.1:n.-131G>C
XR_001740065.1:n.15G>C
XR_940396.2:n.15G>C
NM_001164317.2:c.-131G>C	NP_001157789.1:n.-131G>C
NM_001164318.2:c.-131G>C	NP_001157790.1:n.-131G>C
NM_001164319.2:c.-131G>C	NP_001157791.1:n.-131G>C
NM_001457.4:c.-131G>C MANE Select	NP_001448.2:n.-131G>C