Canonical Allele Identifier: CA1742580510
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1562995726
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843355G>T , CM000669.2:g.128843355G>T GRCh38
NC_000007.13:g.128483409G>T , CM000669.1:g.128483409G>T GRCh37
NC_000007.12:g.128270645G>T NCBI36
NG_011807.1:g.17927G>T , LRG_870:g.17927G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2641+36G>T MANE Select ENSP00000327145.8:n.2641+36G>T
ENST00000325888.12:c.2641+36G>T ENSP00000327145.8:n.2641+36G>T
ENST00000346177.6:c.2641+36G>T ENSP00000344002.6:n.2641+36G>T
NM_001127487.1:c.2641+36G>T NP_001120959.1:n.2641+36G>T
NM_001458.4:c.2641+36G>T , LRG_870t1:c.2641+36G>T NP_001449.3:n.2641+36G>T
NM_001127487.2:c.2641+36G>T NP_001120959.1:n.2641+36G>T
NM_001458.5:c.2641+36G>T MANE Select NP_001449.3:n.2641+36G>T
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