Canonical Allele Identifier: CA437955481
Gene: FGFR3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.1807103T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1805376T>G , CM000666.2:g.1805376T>G GRCh38
NC_000004.11:g.1807103T>G , CM000666.1:g.1807103T>G GRCh37
NC_000004.10:g.1776901T>G NCBI36
NG_012632.1:g.17065T>G , LRG_1021:g.17065T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1440T>G ENSP00000339824.4:p.Leu480=
ENST00000260795.8:c.*490T>G ENSP00000260795.3:n.*490T>G
ENST00000352904.6:c.1098T>G ENSP00000231803.1:p.Leu366=
ENST00000412135.7:c.1422T>G ENSP00000412903.3:p.Leu474=
ENST00000440486.8:c.1434T>G MANE Select ENSP00000414914.2:p.Leu478=
ENST00000481110.7:c.1437T>G ENSP00000420533.2:p.Leu479=
ENST00000260795.6:c.1434T>G ENSP00000260795.2:p.Leu478=
ENST00000340107.8:c.1440T>G ENSP00000339824.4:p.Leu480=
ENST00000352904.5:c.1098T>G ENSP00000231803.1:p.Leu366=
ENST00000412135.6:c.1098T>G ENSP00000412903.2:p.Leu366=
ENST00000440486.6:c.1434T>G ENSP00000414914.2:p.Leu478=
ENST00000469068.1:n.500T>G
ENST00000481110.6:c.1437T>G ENSP00000420533.2:p.Leu479=
ENST00000613647.4:c.*490T>G ENSP00000479472.1:n.*490T>G
NM_000142.4:c.1434T>G , LRG_1021t1:c.1434T>G NP_000133.1:p.Leu478=
NM_001163213.1:c.1440T>G , LRG_1021t2:c.1440T>G NP_001156685.1:p.Leu480=
NM_022965.3:c.1098T>G NP_075254.1:p.Leu366=
XM_006713868.1:c.1446T>G XP_006713931.1:p.Leu482=
XM_006713869.1:c.1446T>G XP_006713932.1:p.Leu482=
XM_006713870.1:c.1443T>G XP_006713933.1:p.Leu481=
XM_006713871.1:c.1440T>G XP_006713934.1:p.Leu480=
XM_006713872.1:c.1437T>G XP_006713935.1:p.Leu479=
XM_006713873.1:c.1434T>G XP_006713936.1:p.Leu478=
XM_011513420.1:c.1440T>G XP_011511722.1:p.Leu480=
XM_011513422.1:c.1437T>G XP_011511724.1:p.Leu479=
NM_001354809.1:c.1437T>G NP_001341738.1:p.Leu479=
NM_001354810.1:c.1437T>G NP_001341739.1:p.Leu479=
NR_148971.1:n.1841T>G
NM_001354809.2:c.1437T>G NP_001341738.1:p.Leu479=
NM_001354810.2:c.1437T>G NP_001341739.1:p.Leu479=
NR_148971.2:n.1860T>G
NM_000142.5:c.1434T>G MANE Select NP_000133.1:p.Leu478=
NM_001163213.2:c.1440T>G NP_001156685.1:p.Leu480=
NM_022965.4:c.1098T>G NP_075254.1:p.Leu366=