Canonical Allele Identifier: CA2684816296
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128843719-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843719C>T , CM000669.2:g.128843719C>T GRCh38
NC_000007.13:g.128483773C>T , CM000669.1:g.128483773C>T GRCh37
NC_000007.12:g.128271009C>T NCBI36
NG_011807.1:g.18291C>T , LRG_870:g.18291C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2812-77C>T MANE Select ENSP00000327145.8:n.2812-77C>T
ENST00000325888.12:c.2812-77C>T ENSP00000327145.8:n.2812-77C>T
ENST00000346177.6:c.2812-77C>T ENSP00000344002.6:n.2812-77C>T
NM_001127487.1:c.2812-77C>T NP_001120959.1:n.2812-77C>T
NM_001458.4:c.2812-77C>T , LRG_870t1:c.2812-77C>T NP_001449.3:n.2812-77C>T
NM_001127487.2:c.2812-77C>T NP_001120959.1:n.2812-77C>T
NM_001458.5:c.2812-77C>T MANE Select NP_001449.3:n.2812-77C>T
Search 100 bp 5'
Search 100 bp 3'