Canonical Allele Identifier: CA355978824
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2249661
ClinVar RCV Id: RCV002787042
dbSNP Id: rs745683500
gnomAD v2: 4-1806063-A-G
gnomAD v3: 4-1804336-A-G
gnomAD v4: 4-1804336-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1804336A>G , CM000666.2:g.1804336A>G GRCh38
NC_000004.11:g.1806063A>G , CM000666.1:g.1806063A>G GRCh37
NC_000004.10:g.1775861A>G NCBI36
NG_012632.1:g.16025A>G , LRG_1021:g.16025A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1088A>G ENSP00000339824.4:p.Glu363Gly
ENST00000260795.8:c.*138A>G ENSP00000260795.3:n.*138A>G
ENST00000352904.6:c.931-488A>G ENSP00000231803.1:n.931-488A>G
ENST00000412135.7:c.1070A>G ENSP00000412903.3:p.Glu357Gly
ENST00000440486.8:c.1082A>G MANE Select ENSP00000414914.2:p.Glu361Gly
ENST00000481110.7:c.1082A>G ENSP00000420533.2:p.Glu361Gly
ENST00000643463.1:n.233A>G
ENST00000260795.6:c.1082A>G ENSP00000260795.2:p.Glu361Gly
ENST00000340107.8:c.1088A>G ENSP00000339824.4:p.Glu363Gly
ENST00000352904.5:c.931-488A>G ENSP00000231803.1:n.931-488A>G
ENST00000412135.6:c.931-488A>G ENSP00000412903.2:n.931-488A>G
ENST00000440486.6:c.1082A>G ENSP00000414914.2:p.Glu361Gly
ENST00000481110.6:c.1082A>G ENSP00000420533.2:p.Glu361Gly
ENST00000613647.4:c.*138A>G ENSP00000479472.1:n.*138A>G
NM_000142.4:c.1082A>G , LRG_1021t1:c.1082A>G NP_000133.1:p.Glu361Gly
NM_001163213.1:c.1088A>G , LRG_1021t2:c.1088A>G NP_001156685.1:p.Glu363Gly
NM_022965.3:c.931-488A>G NP_075254.1:n.931-488A>G
XM_006713868.1:c.1088A>G XP_006713931.1:p.Glu363Gly
XM_006713869.1:c.1088A>G XP_006713932.1:p.Glu363Gly
XM_006713870.1:c.1088A>G XP_006713933.1:p.Glu363Gly
XM_006713871.1:c.1088A>G XP_006713934.1:p.Glu363Gly
XM_006713872.1:c.1082A>G XP_006713935.1:p.Glu361Gly
XM_006713873.1:c.1082A>G XP_006713936.1:p.Glu361Gly
XM_011513420.1:c.1082A>G XP_011511722.1:p.Glu361Gly
XM_011513422.1:c.1082A>G XP_011511724.1:p.Glu361Gly
NM_001354809.1:c.1082A>G NP_001341738.1:p.Glu361Gly
NM_001354810.1:c.1082A>G NP_001341739.1:p.Glu361Gly
NR_148971.1:n.1489A>G
NM_001354809.2:c.1082A>G NP_001341738.1:p.Glu361Gly
NM_001354810.2:c.1082A>G NP_001341739.1:p.Glu361Gly
NR_148971.2:n.1508A>G
NM_000142.5:c.1082A>G MANE Select NP_000133.1:p.Glu361Gly
NM_001163213.2:c.1088A>G NP_001156685.1:p.Glu363Gly
NM_022965.4:c.931-488A>G NP_075254.1:n.931-488A>G