Canonical Allele Identifier: CA253856
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 6400
dbSNP Id: rs121908894

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58077271C>T , CM000665.2:g.58077271C>T GRCh38
NC_000003.11:g.58062998C>T , CM000665.1:g.58062998C>T GRCh37
NC_000003.10:g.58038038C>T NCBI36
NG_012801.1:g.73872C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682097.1:c.518C>T ENSP00000508183.1:p.Ala173Val
ENST00000682868.1:n.661C>T
ENST00000682871.1:c.518C>T ENSP00000507805.1:p.Ala173Val
ENST00000682987.1:n.661C>T
ENST00000683511.1:n.677C>T
ENST00000684107.1:c.518C>T ENSP00000507440.1:p.Ala173Val
ENST00000684506.1:c.518C>T ENSP00000507728.1:p.Ala173Val
ENST00000684517.1:c.518C>T ENSP00000507828.1:p.Ala173Val
ENST00000684607.1:c.518C>T ENSP00000508224.1:p.Ala173Val
ENST00000295956.9:c.518C>T MANE Select ENSP00000295956.5:p.Ala173Val
ENST00000295956.8:c.518C>T ENSP00000295956.4:p.Ala173Val
ENST00000358537.7:c.518C>T ENSP00000351339.3:p.Ala173Val
ENST00000429972.6:c.518C>T ENSP00000415599.2:p.Ala173Val
ENST00000490882.5:c.518C>T ENSP00000420213.1:p.Ala173Val
NM_001164317.1:c.518C>T NP_001157789.1:p.Ala173Val
NM_001164318.1:c.518C>T NP_001157790.1:p.Ala173Val
NM_001164319.1:c.518C>T NP_001157791.1:p.Ala173Val
NM_001457.3:c.518C>T NP_001448.2:p.Ala173Val
XM_005264977.1:c.518C>T XP_005265034.1:p.Ala173Val
XM_005264978.1:c.518C>T XP_005265035.1:p.Ala173Val
XM_005264981.1:c.518C>T XP_005265038.1:p.Ala173Val
XR_940396.1:n.663C>T
XM_005264978.2:c.518C>T XP_005265035.1:p.Ala173Val
XR_001740065.1:n.663C>T
XR_940396.2:n.663C>T
NM_001164317.2:c.518C>T NP_001157789.1:p.Ala173Val
NM_001164318.2:c.518C>T NP_001157790.1:p.Ala173Val
NM_001164319.2:c.518C>T NP_001157791.1:p.Ala173Val
NM_001457.4:c.518C>T MANE Select NP_001448.2:p.Ala173Val