Canonical Allele Identifier: CA2982739
Gene: FGF5 HGNC NCBI

Linked Data

dbSNP Id: rs767703366
gnomAD v2: 4-81207729-A-G
gnomAD v3: 4-80286575-A-G
gnomAD v4: 4-80286575-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286575A>G , CM000666.2:g.80286575A>G GRCh38
NC_000004.11:g.81207729A>G , CM000666.1:g.81207729A>G GRCh37
NC_000004.10:g.81426753A>G NCBI36
NG_029501.1:g.24988A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.710A>G MANE Select ENSP00000311697.7:p.Lys237Arg
ENST00000312465.11:c.710A>G ENSP00000311697.7:p.Lys237Arg
ENST00000456523.3:c.*234A>G ENSP00000398353.3:n.*234A>G
ENST00000503413.1:n.659A>G
ENST00000507780.1:c.342+11563A>G ENSP00000423903.1:n.342+11563A>G
NM_001291812.1:c.281A>G NP_001278741.1:p.Lys94Arg
NM_004464.3:c.710A>G NP_004455.2:p.Lys237Arg
NM_033143.2:c.*234A>G NP_149134.1:n.*234A>G
NM_001291812.2:c.281A>G NP_001278741.1:p.Lys94Arg
NM_004464.4:c.710A>G MANE Select NP_004455.2:p.Lys237Arg