Canonical Allele Identifier: CA457577483
Gene: FLNC HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128483300C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843246C>G , CM000669.2:g.128843246C>G GRCh38
NC_000007.13:g.128483300C>G , CM000669.1:g.128483300C>G GRCh37
NC_000007.12:g.128270536C>G NCBI36
NG_011807.1:g.17818C>G , LRG_870:g.17818C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2568C>G MANE Select ENSP00000327145.8:p.Pro856=
ENST00000325888.12:c.2568C>G ENSP00000327145.8:p.Pro856=
ENST00000346177.6:c.2568C>G ENSP00000344002.6:p.Pro856=
NM_001127487.1:c.2568C>G NP_001120959.1:p.Pro856=
NM_001458.4:c.2568C>G , LRG_870t1:c.2568C>G NP_001449.3:p.Pro856=
NM_001127487.2:c.2568C>G NP_001120959.1:p.Pro856=
NM_001458.5:c.2568C>G MANE Select NP_001449.3:p.Pro856=
Search 100 bp 5'
Search 100 bp 3'