Canonical Allele Identifier: CA2809727
Gene: FGFR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 283366
ClinVar RCV Id: RCV000404567
dbSNP Id: rs750641928

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1799294C>T , CM000666.2:g.1799294C>T GRCh38
NC_000004.11:g.1801021C>T , CM000666.1:g.1801021C>T GRCh37
NC_000004.10:g.1770819C>T NCBI36
NG_012632.1:g.10983C>T , LRG_1021:g.10983C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260795.8:c.150C>T ENSP00000260795.3:p.Val50=
ENST00000352904.6:c.150C>T ENSP00000231803.1:p.Val50=
ENST00000412135.7:c.150C>T ENSP00000412903.3:p.Val50=
ENST00000440486.8:c.150C>T MANE Select ENSP00000414914.2:p.Val50=
ENST00000481110.7:c.150C>T ENSP00000420533.2:p.Val50=
ENST00000260795.6:c.150C>T ENSP00000260795.2:p.Val50=
ENST00000340107.8:c.150C>T ENSP00000339824.4:p.Val50=
ENST00000352904.5:c.150C>T ENSP00000231803.1:p.Val50=
ENST00000412135.6:c.150C>T ENSP00000412903.2:p.Val50=
ENST00000440486.6:c.150C>T ENSP00000414914.2:p.Val50=
ENST00000481110.6:c.150C>T ENSP00000420533.2:p.Val50=
ENST00000613647.4:c.150C>T ENSP00000479472.1:p.Val50=
NM_000142.4:c.150C>T , LRG_1021t1:c.150C>T NP_000133.1:p.Val50=
NM_001163213.1:c.150C>T , LRG_1021t2:c.150C>T NP_001156685.1:p.Val50=
NM_022965.3:c.150C>T NP_075254.1:p.Val50=
XM_006713868.1:c.150C>T XP_006713931.1:p.Val50=
XM_006713869.1:c.150C>T XP_006713932.1:p.Val50=
XM_006713870.1:c.150C>T XP_006713933.1:p.Val50=
XM_006713871.1:c.150C>T XP_006713934.1:p.Val50=
XM_006713872.1:c.150C>T XP_006713935.1:p.Val50=
XM_006713873.1:c.150C>T XP_006713936.1:p.Val50=
XM_011513420.1:c.150C>T XP_011511722.1:p.Val50=
XM_011513422.1:c.150C>T XP_011511724.1:p.Val50=
NM_001354809.1:c.150C>T NP_001341738.1:p.Val50=
NM_001354810.1:c.150C>T NP_001341739.1:p.Val50=
NR_148971.1:n.406C>T
NM_001354809.2:c.150C>T NP_001341738.1:p.Val50=
NM_001354810.2:c.150C>T NP_001341739.1:p.Val50=
NR_148971.2:n.425C>T
NM_000142.5:c.150C>T MANE Select NP_000133.1:p.Val50=
NM_001163213.2:c.150C>T NP_001156685.1:p.Val50=
NM_022965.4:c.150C>T NP_075254.1:p.Val50=