Canonical Allele Identifier: CA355979113

Gene: FGFR3

Linked Data

• dbSNP Id: rs2108797339
• MyVariant Identifiers: chr4:g.1806141T>G (hg19) ; chr4:g.1804414T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804414T>G , CM000666.2:g.1804414T>G	GRCh38
NC_000004.11:g.1806141T>G , CM000666.1:g.1806141T>G	GRCh37
NC_000004.10:g.1775939T>G	NCBI36
NG_012632.1:g.16103T>G , LRG_1021:g.16103T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1166T>G	ENSP00000339824.4:p.Ile389Ser
ENST00000260795.8:c.*216T>G	ENSP00000260795.3:n.*216T>G
ENST00000352904.6:c.931-410T>G	ENSP00000231803.1:n.931-410T>G
ENST00000412135.7:c.1148T>G	ENSP00000412903.3:p.Ile383Ser
ENST00000440486.8:c.1160T>G MANE Select	ENSP00000414914.2:p.Ile387Ser
ENST00000481110.7:c.1160T>G	ENSP00000420533.2:p.Ile387Ser
ENST00000643463.1:n.311T>G
ENST00000260795.6:c.1160T>G	ENSP00000260795.2:p.Ile387Ser
ENST00000340107.8:c.1166T>G	ENSP00000339824.4:p.Ile389Ser
ENST00000352904.5:c.931-410T>G	ENSP00000231803.1:n.931-410T>G
ENST00000412135.6:c.931-410T>G	ENSP00000412903.2:n.931-410T>G
ENST00000440486.6:c.1160T>G	ENSP00000414914.2:p.Ile387Ser
ENST00000481110.6:c.1160T>G	ENSP00000420533.2:p.Ile387Ser
ENST00000613647.4:c.*216T>G	ENSP00000479472.1:n.*216T>G
NM_000142.4:c.1160T>G , LRG_1021t1:c.1160T>G	NP_000133.1:p.Ile387Ser
NM_001163213.1:c.1166T>G , LRG_1021t2:c.1166T>G	NP_001156685.1:p.Ile389Ser
NM_022965.3:c.931-410T>G	NP_075254.1:n.931-410T>G
XM_006713868.1:c.1166T>G	XP_006713931.1:p.Ile389Ser
XM_006713869.1:c.1166T>G	XP_006713932.1:p.Ile389Ser
XM_006713870.1:c.1166T>G	XP_006713933.1:p.Ile389Ser
XM_006713871.1:c.1166T>G	XP_006713934.1:p.Ile389Ser
XM_006713872.1:c.1160T>G	XP_006713935.1:p.Ile387Ser
XM_006713873.1:c.1160T>G	XP_006713936.1:p.Ile387Ser
XM_011513420.1:c.1160T>G	XP_011511722.1:p.Ile387Ser
XM_011513422.1:c.1160T>G	XP_011511724.1:p.Ile387Ser
NM_001354809.1:c.1160T>G	NP_001341738.1:p.Ile387Ser
NM_001354810.1:c.1160T>G	NP_001341739.1:p.Ile387Ser
NR_148971.1:n.1567T>G
NM_001354809.2:c.1160T>G	NP_001341738.1:p.Ile387Ser
NM_001354810.2:c.1160T>G	NP_001341739.1:p.Ile387Ser
NR_148971.2:n.1586T>G
NM_000142.5:c.1160T>G MANE Select	NP_000133.1:p.Ile387Ser
NM_001163213.2:c.1166T>G	NP_001156685.1:p.Ile389Ser
NM_022965.4:c.931-410T>G	NP_075254.1:n.931-410T>G