Canonical Allele Identifier: CA437955074

Gene: FGFR3

Linked Data

• dbSNP Id: rs1418835941
• gnomAD v2: 4-1806121-G-A
• gnomAD v4: 4-1804394-G-A
• MyVariant Identifiers: chr4:g.1806121G>A (hg19) ; chr4:g.1804394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804394G>A , CM000666.2:g.1804394G>A	GRCh38
NC_000004.11:g.1806121G>A , CM000666.1:g.1806121G>A	GRCh37
NC_000004.10:g.1775919G>A	NCBI36
NG_012632.1:g.16083G>A , LRG_1021:g.16083G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1146G>A	ENSP00000339824.4:p.Gly382=
ENST00000260795.8:c.*196G>A	ENSP00000260795.3:n.*196G>A
ENST00000352904.6:c.931-430G>A	ENSP00000231803.1:n.931-430G>A
ENST00000412135.7:c.1128G>A	ENSP00000412903.3:p.Gly376=
ENST00000440486.8:c.1140G>A MANE Select	ENSP00000414914.2:p.Gly380=
ENST00000481110.7:c.1140G>A	ENSP00000420533.2:p.Gly380=
ENST00000643463.1:n.291G>A
ENST00000260795.6:c.1140G>A	ENSP00000260795.2:p.Gly380=
ENST00000340107.8:c.1146G>A	ENSP00000339824.4:p.Gly382=
ENST00000352904.5:c.931-430G>A	ENSP00000231803.1:n.931-430G>A
ENST00000412135.6:c.931-430G>A	ENSP00000412903.2:n.931-430G>A
ENST00000440486.6:c.1140G>A	ENSP00000414914.2:p.Gly380=
ENST00000481110.6:c.1140G>A	ENSP00000420533.2:p.Gly380=
ENST00000613647.4:c.*196G>A	ENSP00000479472.1:n.*196G>A
NM_000142.4:c.1140G>A , LRG_1021t1:c.1140G>A	NP_000133.1:p.Gly380=
NM_001163213.1:c.1146G>A , LRG_1021t2:c.1146G>A	NP_001156685.1:p.Gly382=
NM_022965.3:c.931-430G>A	NP_075254.1:n.931-430G>A
XM_006713868.1:c.1146G>A	XP_006713931.1:p.Gly382=
XM_006713869.1:c.1146G>A	XP_006713932.1:p.Gly382=
XM_006713870.1:c.1146G>A	XP_006713933.1:p.Gly382=
XM_006713871.1:c.1146G>A	XP_006713934.1:p.Gly382=
XM_006713872.1:c.1140G>A	XP_006713935.1:p.Gly380=
XM_006713873.1:c.1140G>A	XP_006713936.1:p.Gly380=
XM_011513420.1:c.1140G>A	XP_011511722.1:p.Gly380=
XM_011513422.1:c.1140G>A	XP_011511724.1:p.Gly380=
NM_001354809.1:c.1140G>A	NP_001341738.1:p.Gly380=
NM_001354810.1:c.1140G>A	NP_001341739.1:p.Gly380=
NR_148971.1:n.1547G>A
NM_001354809.2:c.1140G>A	NP_001341738.1:p.Gly380=
NM_001354810.2:c.1140G>A	NP_001341739.1:p.Gly380=
NR_148971.2:n.1566G>A
NM_000142.5:c.1140G>A MANE Select	NP_000133.1:p.Gly380=
NM_001163213.2:c.1146G>A	NP_001156685.1:p.Gly382=
NM_022965.4:c.931-430G>A	NP_075254.1:n.931-430G>A