Canonical Allele Identifier: CA2810286

Gene: FGFR3

Linked Data

• ClinVar Variation Id: 1254355
• ClinVar RCV Id: RCV001653137 ; RCV002538541
• dbSNP Id: rs370064407
• ExAC: 4:1806176 C / T
• gnomAD v2: 4-1806176-C-T
• gnomAD v3: 4-1804449-C-T
• gnomAD v4: 4-1804449-C-T
• COSMIC: COSM296687
• MyVariant Identifiers: chr4:g.1806176C>T (hg19) ; chr4:g.1804449C>T (hg38)
• CIViC: CA2810286

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804449C>T , CM000666.2:g.1804449C>T	GRCh38
NC_000004.11:g.1806176C>T , CM000666.1:g.1806176C>T	GRCh37
NC_000004.10:g.1775974C>T	NCBI36
NG_012632.1:g.16138C>T , LRG_1021:g.16138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1201C>T	ENSP00000339824.4:p.Arg401Cys
ENST00000260795.8:c.*251C>T	ENSP00000260795.3:n.*251C>T
ENST00000352904.6:c.931-375C>T	ENSP00000231803.1:n.931-375C>T
ENST00000412135.7:c.1183C>T	ENSP00000412903.3:p.Arg395Cys
ENST00000440486.8:c.1195C>T MANE Select	ENSP00000414914.2:p.Arg399Cys
ENST00000481110.7:c.1195C>T	ENSP00000420533.2:p.Arg399Cys
ENST00000643463.1:n.346C>T
ENST00000260795.6:c.1195C>T	ENSP00000260795.2:p.Arg399Cys
ENST00000340107.8:c.1201C>T	ENSP00000339824.4:p.Arg401Cys
ENST00000352904.5:c.931-375C>T	ENSP00000231803.1:n.931-375C>T
ENST00000412135.6:c.931-375C>T	ENSP00000412903.2:n.931-375C>T
ENST00000440486.6:c.1195C>T	ENSP00000414914.2:p.Arg399Cys
ENST00000481110.6:c.1195C>T	ENSP00000420533.2:p.Arg399Cys
ENST00000613647.4:c.*251C>T	ENSP00000479472.1:n.*251C>T
NM_000142.4:c.1195C>T , LRG_1021t1:c.1195C>T	NP_000133.1:p.Arg399Cys
NM_001163213.1:c.1201C>T , LRG_1021t2:c.1201C>T	NP_001156685.1:p.Arg401Cys
NM_022965.3:c.931-375C>T	NP_075254.1:n.931-375C>T
XM_006713868.1:c.1201C>T	XP_006713931.1:p.Arg401Cys
XM_006713869.1:c.1201C>T	XP_006713932.1:p.Arg401Cys
XM_006713870.1:c.1201C>T	XP_006713933.1:p.Arg401Cys
XM_006713871.1:c.1201C>T	XP_006713934.1:p.Arg401Cys
XM_006713872.1:c.1195C>T	XP_006713935.1:p.Arg399Cys
XM_006713873.1:c.1195C>T	XP_006713936.1:p.Arg399Cys
XM_011513420.1:c.1195C>T	XP_011511722.1:p.Arg399Cys
XM_011513422.1:c.1195C>T	XP_011511724.1:p.Arg399Cys
NM_001354809.1:c.1195C>T	NP_001341738.1:p.Arg399Cys
NM_001354810.1:c.1195C>T	NP_001341739.1:p.Arg399Cys
NR_148971.1:n.1602C>T
NM_001354809.2:c.1195C>T	NP_001341738.1:p.Arg399Cys
NM_001354810.2:c.1195C>T	NP_001341739.1:p.Arg399Cys
NR_148971.2:n.1621C>T
NM_000142.5:c.1195C>T MANE Select	NP_000133.1:p.Arg399Cys
NM_001163213.2:c.1201C>T	NP_001156685.1:p.Arg401Cys
NM_022965.4:c.931-375C>T	NP_075254.1:n.931-375C>T