Canonical Allele Identifier: CA4474125
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs750082280
ExAC: 7:128477556 T / C
gnomAD v2: 7-128477556-T-C
gnomAD v3: 7-128837502-T-C
gnomAD v4: 7-128837502-T-C
MyVariant Identifiers: chr7:g.128477556T>C (hg19) chr7:g.128837502T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128837502T>C , CM000669.2:g.128837502T>C GRCh38
NC_000007.13:g.128477556T>C , CM000669.1:g.128477556T>C GRCh37
NC_000007.12:g.128264792T>C NCBI36
NG_011807.1:g.12074T>C , LRG_870:g.12074T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.804T>C MANE Select ENSP00000327145.8:p.Val268=
ENST00000325888.12:c.804T>C ENSP00000327145.8:p.Val268=
ENST00000346177.6:c.804T>C ENSP00000344002.6:p.Val268=
NM_001127487.1:c.804T>C NP_001120959.1:p.Val268=
NM_001458.4:c.804T>C , LRG_870t1:c.804T>C NP_001449.3:p.Val268=
NM_001127487.2:c.804T>C NP_001120959.1:p.Val268=
NM_001458.5:c.804T>C MANE Select NP_001449.3:p.Val268=
Search 100 bp 5'
Search 100 bp 3'