Canonical Allele Identifier: CA369227369
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128841278-A-C
MyVariant Identifiers: chr7:g.128481332A>C (hg19) chr7:g.128841278A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841278A>C , CM000669.2:g.128841278A>C GRCh38
NC_000007.13:g.128481332A>C , CM000669.1:g.128481332A>C GRCh37
NC_000007.12:g.128268568A>C NCBI36
NG_011807.1:g.15850A>C , LRG_870:g.15850A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1922A>C MANE Select ENSP00000327145.8:p.His641Pro
ENST00000325888.12:c.1922A>C ENSP00000327145.8:p.His641Pro
ENST00000346177.6:c.1922A>C ENSP00000344002.6:p.His641Pro
NM_001127487.1:c.1922A>C NP_001120959.1:p.His641Pro
NM_001458.4:c.1922A>C , LRG_870t1:c.1922A>C NP_001449.3:p.His641Pro
NM_001127487.2:c.1922A>C NP_001120959.1:p.His641Pro
NM_001458.5:c.1922A>C MANE Select NP_001449.3:p.His641Pro
Search 100 bp 5'
Search 100 bp 3'