Canonical Allele Identifier: CA344898

Gene: FGFR3

Linked Data

• ClinVar Variation Id: 65564
• ClinVar RCV Id: RCV000055766 ; RCV001569868
• dbSNP Id: rs121913103
• MyVariant Identifiers: chr4:g.1808989A>G (hg19) ; chr4:g.1807262A>G (hg38)
• PubMed: PMID:20301540

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1807262A>G , CM000666.2:g.1807262A>G	GRCh38
NC_000004.11:g.1808989A>G , CM000666.1:g.1808989A>G	GRCh37
NC_000004.10:g.1778787A>G	NCBI36
NG_012632.1:g.18951A>G , LRG_1021:g.18951A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.2427A>G	ENSP00000339824.4:p.Ter809Trp
ENST00000260795.8:c.*1477A>G	ENSP00000260795.3:n.*1477A>G
ENST00000352904.6:c.2085A>G	ENSP00000231803.1:p.Ter695Trp
ENST00000412135.7:c.2409A>G	ENSP00000412903.3:p.Ter803Trp
ENST00000440486.8:c.2421A>G MANE Select	ENSP00000414914.2:p.Ter807Trp
ENST00000481110.7:c.2353A>G	ENSP00000420533.2:p.Lys785Glu
ENST00000260795.6:c.2421A>G	ENSP00000260795.2:p.Ter807Trp
ENST00000340107.8:c.2427A>G	ENSP00000339824.4:p.Ter809Trp
ENST00000352904.5:c.2085A>G	ENSP00000231803.1:p.Ter695Trp
ENST00000412135.6:c.2085A>G	ENSP00000412903.2:p.Ter695Trp
ENST00000440486.6:c.2421A>G	ENSP00000414914.2:p.Ter807Trp
ENST00000481110.6:c.2353A>G	ENSP00000420533.2:p.Lys785Glu
ENST00000613647.4:c.*1477A>G	ENSP00000479472.1:n.*1477A>G
NM_000142.4:c.2421A>G , LRG_1021t1:c.2421A>G	NP_000133.1:p.Ter807Trp
NM_001163213.1:c.2427A>G , LRG_1021t2:c.2427A>G	NP_001156685.1:p.Ter809Trp
NM_022965.3:c.2085A>G	NP_075254.1:p.Ter695Trp
XM_006713868.1:c.2436A>G	XP_006713931.1:p.Ter812Trp
XM_006713869.1:c.2433A>G	XP_006713932.1:p.Ter811Trp
XM_006713870.1:c.2433A>G	XP_006713933.1:p.Ter811Trp
XM_006713871.1:c.2430A>G	XP_006713934.1:p.Ter810Trp
XM_006713872.1:c.2424A>G	XP_006713935.1:p.Ter808Trp
XM_006713873.1:c.2424A>G	XP_006713936.1:p.Ter808Trp
XM_011513420.1:c.2430A>G	XP_011511722.1:p.Ter810Trp
XM_011513422.1:c.2427A>G	XP_011511724.1:p.Ter809Trp
NM_001354809.1:c.2424A>G	NP_001341738.1:p.Ter808Trp
NM_001354810.1:c.2353A>G	NP_001341739.1:p.Lys785Glu
NR_148971.1:n.2828A>G
NM_001354809.2:c.2424A>G	NP_001341738.1:p.Ter808Trp
NM_001354810.2:c.2353A>G	NP_001341739.1:p.Lys785Glu
NR_148971.2:n.2847A>G
NM_000142.5:c.2421A>G MANE Select	NP_000133.1:p.Ter807Trp
NM_001163213.2:c.2427A>G	NP_001156685.1:p.Ter809Trp
NM_022965.4:c.2085A>G	NP_075254.1:p.Ter695Trp