Canonical Allele Identifier: CA355979075

Gene: FGFR3

Linked Data

• dbSNP Id: rs200186825
• gnomAD v2: 4-1806134-C-G
• gnomAD v3: 4-1804407-C-G
• gnomAD v4: 4-1804407-C-G
• MyVariant Identifiers: chr4:g.1806134C>G (hg19) ; chr4:g.1804407C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804407C>G , CM000666.2:g.1804407C>G	GRCh38
NC_000004.11:g.1806134C>G , CM000666.1:g.1806134C>G	GRCh37
NC_000004.10:g.1775932C>G	NCBI36
NG_012632.1:g.16096C>G , LRG_1021:g.16096C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1159C>G	ENSP00000339824.4:p.Leu387Val
ENST00000260795.8:c.*209C>G	ENSP00000260795.3:n.*209C>G
ENST00000352904.6:c.931-417C>G	ENSP00000231803.1:n.931-417C>G
ENST00000412135.7:c.1141C>G	ENSP00000412903.3:p.Leu381Val
ENST00000440486.8:c.1153C>G MANE Select	ENSP00000414914.2:p.Leu385Val
ENST00000481110.7:c.1153C>G	ENSP00000420533.2:p.Leu385Val
ENST00000643463.1:n.304C>G
ENST00000260795.6:c.1153C>G	ENSP00000260795.2:p.Leu385Val
ENST00000340107.8:c.1159C>G	ENSP00000339824.4:p.Leu387Val
ENST00000352904.5:c.931-417C>G	ENSP00000231803.1:n.931-417C>G
ENST00000412135.6:c.931-417C>G	ENSP00000412903.2:n.931-417C>G
ENST00000440486.6:c.1153C>G	ENSP00000414914.2:p.Leu385Val
ENST00000481110.6:c.1153C>G	ENSP00000420533.2:p.Leu385Val
ENST00000613647.4:c.*209C>G	ENSP00000479472.1:n.*209C>G
NM_000142.4:c.1153C>G , LRG_1021t1:c.1153C>G	NP_000133.1:p.Leu385Val
NM_001163213.1:c.1159C>G , LRG_1021t2:c.1159C>G	NP_001156685.1:p.Leu387Val
NM_022965.3:c.931-417C>G	NP_075254.1:n.931-417C>G
XM_006713868.1:c.1159C>G	XP_006713931.1:p.Leu387Val
XM_006713869.1:c.1159C>G	XP_006713932.1:p.Leu387Val
XM_006713870.1:c.1159C>G	XP_006713933.1:p.Leu387Val
XM_006713871.1:c.1159C>G	XP_006713934.1:p.Leu387Val
XM_006713872.1:c.1153C>G	XP_006713935.1:p.Leu385Val
XM_006713873.1:c.1153C>G	XP_006713936.1:p.Leu385Val
XM_011513420.1:c.1153C>G	XP_011511722.1:p.Leu385Val
XM_011513422.1:c.1153C>G	XP_011511724.1:p.Leu385Val
NM_001354809.1:c.1153C>G	NP_001341738.1:p.Leu385Val
NM_001354810.1:c.1153C>G	NP_001341739.1:p.Leu385Val
NR_148971.1:n.1560C>G
NM_001354809.2:c.1153C>G	NP_001341738.1:p.Leu385Val
NM_001354810.2:c.1153C>G	NP_001341739.1:p.Leu385Val
NR_148971.2:n.1579C>G
NM_000142.5:c.1153C>G MANE Select	NP_000133.1:p.Leu385Val
NM_001163213.2:c.1159C>G	NP_001156685.1:p.Leu387Val
NM_022965.4:c.931-417C>G	NP_075254.1:n.931-417C>G