Canonical Allele Identifier: CA355982289

Gene: FGFR3

Linked Data

• dbSNP Id: rs753541491
• MyVariant Identifiers: chr4:g.1807797C>T (hg19) ; chr4:g.1806070C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1806070C>T , CM000666.2:g.1806070C>T	GRCh38
NC_000004.11:g.1807797C>T , CM000666.1:g.1807797C>T	GRCh37
NC_000004.10:g.1777595C>T	NCBI36
NG_012632.1:g.17759C>T , LRG_1021:g.17759C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1862C>T	ENSP00000339824.4:p.Ala621Val
ENST00000260795.8:c.*912C>T	ENSP00000260795.3:n.*912C>T
ENST00000352904.6:c.1520C>T	ENSP00000231803.1:p.Ala507Val
ENST00000412135.7:c.1844C>T	ENSP00000412903.3:p.Ala615Val
ENST00000440486.8:c.1856C>T MANE Select	ENSP00000414914.2:p.Ala619Val
ENST00000481110.7:c.1859C>T	ENSP00000420533.2:p.Ala620Val
ENST00000260795.6:c.1856C>T	ENSP00000260795.2:p.Ala619Val
ENST00000340107.8:c.1862C>T	ENSP00000339824.4:p.Ala621Val
ENST00000352904.5:c.1520C>T	ENSP00000231803.1:p.Ala507Val
ENST00000412135.6:c.1520C>T	ENSP00000412903.2:p.Ala507Val
ENST00000440486.6:c.1856C>T	ENSP00000414914.2:p.Ala619Val
ENST00000481110.6:c.1859C>T	ENSP00000420533.2:p.Ala620Val
ENST00000613647.4:c.*912C>T	ENSP00000479472.1:n.*912C>T
NM_000142.4:c.1856C>T , LRG_1021t1:c.1856C>T	NP_000133.1:p.Ala619Val
NM_001163213.1:c.1862C>T , LRG_1021t2:c.1862C>T	NP_001156685.1:p.Ala621Val
NM_022965.3:c.1520C>T	NP_075254.1:p.Ala507Val
XM_006713868.1:c.1868C>T	XP_006713931.1:p.Ala623Val
XM_006713869.1:c.1868C>T	XP_006713932.1:p.Ala623Val
XM_006713870.1:c.1865C>T	XP_006713933.1:p.Ala622Val
XM_006713871.1:c.1862C>T	XP_006713934.1:p.Ala621Val
XM_006713872.1:c.1859C>T	XP_006713935.1:p.Ala620Val
XM_006713873.1:c.1856C>T	XP_006713936.1:p.Ala619Val
XM_011513420.1:c.1862C>T	XP_011511722.1:p.Ala621Val
XM_011513422.1:c.1859C>T	XP_011511724.1:p.Ala620Val
NM_001354809.1:c.1859C>T	NP_001341738.1:p.Ala620Val
NM_001354810.1:c.1859C>T	NP_001341739.1:p.Ala620Val
NR_148971.1:n.2263C>T
NM_001354809.2:c.1859C>T	NP_001341738.1:p.Ala620Val
NM_001354810.2:c.1859C>T	NP_001341739.1:p.Ala620Val
NR_148971.2:n.2282C>T
NM_000142.5:c.1856C>T MANE Select	NP_000133.1:p.Ala619Val
NM_001163213.2:c.1862C>T	NP_001156685.1:p.Ala621Val
NM_022965.4:c.1520C>T	NP_075254.1:p.Ala507Val