Canonical Allele Identifier: CA91253903

Gene: FGFR3

Linked Data

• ClinVar Variation Id: 1800763
• ClinVar RCV Id: RCV002462360
• dbSNP Id: rs11943863
• gnomAD v3: 4-1804402-T-G
• gnomAD v4: 4-1804402-T-G
• MyVariant Identifiers: chr4:g.1806129T>G (hg19) ; chr4:g.1804402T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804402T>G , CM000666.2:g.1804402T>G	GRCh38
NC_000004.11:g.1806129T>G , CM000666.1:g.1806129T>G	GRCh37
NC_000004.10:g.1775927T>G	NCBI36
NG_012632.1:g.16091T>G , LRG_1021:g.16091T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1154T>G	ENSP00000339824.4:p.Phe385Cys
ENST00000260795.8:c.*204T>G	ENSP00000260795.3:n.*204T>G
ENST00000352904.6:c.931-422T>G	ENSP00000231803.1:n.931-422T>G
ENST00000412135.7:c.1136T>G	ENSP00000412903.3:p.Phe379Cys
ENST00000440486.8:c.1148T>G MANE Select	ENSP00000414914.2:p.Phe383Cys
ENST00000481110.7:c.1148T>G	ENSP00000420533.2:p.Phe383Cys
ENST00000643463.1:n.299T>G
ENST00000260795.6:c.1148T>G	ENSP00000260795.2:p.Phe383Cys
ENST00000340107.8:c.1154T>G	ENSP00000339824.4:p.Phe385Cys
ENST00000352904.5:c.931-422T>G	ENSP00000231803.1:n.931-422T>G
ENST00000412135.6:c.931-422T>G	ENSP00000412903.2:n.931-422T>G
ENST00000440486.6:c.1148T>G	ENSP00000414914.2:p.Phe383Cys
ENST00000481110.6:c.1148T>G	ENSP00000420533.2:p.Phe383Cys
ENST00000613647.4:c.*204T>G	ENSP00000479472.1:n.*204T>G
NM_000142.4:c.1148T>G , LRG_1021t1:c.1148T>G	NP_000133.1:p.Phe383Cys
NM_001163213.1:c.1154T>G , LRG_1021t2:c.1154T>G	NP_001156685.1:p.Phe385Cys
NM_022965.3:c.931-422T>G	NP_075254.1:n.931-422T>G
XM_006713868.1:c.1154T>G	XP_006713931.1:p.Phe385Cys
XM_006713869.1:c.1154T>G	XP_006713932.1:p.Phe385Cys
XM_006713870.1:c.1154T>G	XP_006713933.1:p.Phe385Cys
XM_006713871.1:c.1154T>G	XP_006713934.1:p.Phe385Cys
XM_006713872.1:c.1148T>G	XP_006713935.1:p.Phe383Cys
XM_006713873.1:c.1148T>G	XP_006713936.1:p.Phe383Cys
XM_011513420.1:c.1148T>G	XP_011511722.1:p.Phe383Cys
XM_011513422.1:c.1148T>G	XP_011511724.1:p.Phe383Cys
NM_001354809.1:c.1148T>G	NP_001341738.1:p.Phe383Cys
NM_001354810.1:c.1148T>G	NP_001341739.1:p.Phe383Cys
NR_148971.1:n.1555T>G
NM_001354809.2:c.1148T>G	NP_001341738.1:p.Phe383Cys
NM_001354810.2:c.1148T>G	NP_001341739.1:p.Phe383Cys
NR_148971.2:n.1574T>G
NM_000142.5:c.1148T>G MANE Select	NP_000133.1:p.Phe383Cys
NM_001163213.2:c.1154T>G	NP_001156685.1:p.Phe385Cys
NM_022965.4:c.931-422T>G	NP_075254.1:n.931-422T>G