Canonical Allele Identifier: CA355982361

Gene: FGFR3

Linked Data

• dbSNP Id: rs778449048
• MyVariant Identifiers: chr4:g.1807817A>C (hg19) ; chr4:g.1806090A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1806090A>C , CM000666.2:g.1806090A>C	GRCh38
NC_000004.11:g.1807817A>C , CM000666.1:g.1807817A>C	GRCh37
NC_000004.10:g.1777615A>C	NCBI36
NG_012632.1:g.17779A>C , LRG_1021:g.17779A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1882A>C	ENSP00000339824.4:p.Thr628Pro
ENST00000260795.8:c.*932A>C	ENSP00000260795.3:n.*932A>C
ENST00000352904.6:c.1540A>C	ENSP00000231803.1:p.Thr514Pro
ENST00000412135.7:c.1864A>C	ENSP00000412903.3:p.Thr622Pro
ENST00000440486.8:c.1876A>C MANE Select	ENSP00000414914.2:p.Thr626Pro
ENST00000481110.7:c.1879A>C	ENSP00000420533.2:p.Thr627Pro
ENST00000260795.6:c.1876A>C	ENSP00000260795.2:p.Thr626Pro
ENST00000340107.8:c.1882A>C	ENSP00000339824.4:p.Thr628Pro
ENST00000352904.5:c.1540A>C	ENSP00000231803.1:p.Thr514Pro
ENST00000412135.6:c.1540A>C	ENSP00000412903.2:p.Thr514Pro
ENST00000440486.6:c.1876A>C	ENSP00000414914.2:p.Thr626Pro
ENST00000481110.6:c.1879A>C	ENSP00000420533.2:p.Thr627Pro
ENST00000613647.4:c.*932A>C	ENSP00000479472.1:n.*932A>C
NM_000142.4:c.1876A>C , LRG_1021t1:c.1876A>C	NP_000133.1:p.Thr626Pro
NM_001163213.1:c.1882A>C , LRG_1021t2:c.1882A>C	NP_001156685.1:p.Thr628Pro
NM_022965.3:c.1540A>C	NP_075254.1:p.Thr514Pro
XM_006713868.1:c.1888A>C	XP_006713931.1:p.Thr630Pro
XM_006713869.1:c.1888A>C	XP_006713932.1:p.Thr630Pro
XM_006713870.1:c.1885A>C	XP_006713933.1:p.Thr629Pro
XM_006713871.1:c.1882A>C	XP_006713934.1:p.Thr628Pro
XM_006713872.1:c.1879A>C	XP_006713935.1:p.Thr627Pro
XM_006713873.1:c.1876A>C	XP_006713936.1:p.Thr626Pro
XM_011513420.1:c.1882A>C	XP_011511722.1:p.Thr628Pro
XM_011513422.1:c.1879A>C	XP_011511724.1:p.Thr627Pro
NM_001354809.1:c.1879A>C	NP_001341738.1:p.Thr627Pro
NM_001354810.1:c.1879A>C	NP_001341739.1:p.Thr627Pro
NR_148971.1:n.2283A>C
NM_001354809.2:c.1879A>C	NP_001341738.1:p.Thr627Pro
NM_001354810.2:c.1879A>C	NP_001341739.1:p.Thr627Pro
NR_148971.2:n.2302A>C
NM_000142.5:c.1876A>C MANE Select	NP_000133.1:p.Thr626Pro
NM_001163213.2:c.1882A>C	NP_001156685.1:p.Thr628Pro
NM_022965.4:c.1540A>C	NP_075254.1:p.Thr514Pro