Canonical Allele Identifier: CA362286825
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs2149731698

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177090943T>C , CM000667.2:g.177090943T>C GRCh38
NC_000005.9:g.176517944T>C , CM000667.1:g.176517944T>C GRCh37
NC_000005.8:g.176450550T>C NCBI36
NG_012067.1:g.9024T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.442T>C MANE Select ENSP00000292408.4:p.Tyr148His
ENST00000292408.8:c.442T>C ENSP00000292408.4:p.Tyr148His
ENST00000393637.5:c.442T>C ENSP00000377254.1:p.Tyr148His
ENST00000393648.6:c.442T>C ENSP00000377259.2:p.Tyr148His
ENST00000426612.5:n.559T>C
ENST00000430285.5:c.*306T>C ENSP00000395164.1:n.*306T>C
ENST00000502906.5:c.442T>C ENSP00000424960.1:p.Tyr148His
ENST00000503708.5:c.442T>C ENSP00000424905.1:p.Tyr148His
ENST00000509511.5:n.442T>C
NM_001291980.1:c.442T>C NP_001278909.1:p.Tyr148His
NM_002011.4:c.442T>C NP_002002.3:p.Tyr148His
NM_022963.3:c.442T>C NP_075252.2:p.Tyr148His
NM_213647.2:c.442T>C NP_998812.1:p.Tyr148His
XM_005265838.2:c.442T>C XP_005265895.1:p.Tyr148His
XM_011534464.1:c.535T>C XP_011532766.1:p.Tyr179His
XM_011534465.1:c.124T>C XP_011532767.1:p.Tyr42His
XR_941090.1:n.487T>C
NM_001354984.1:c.442T>C NP_001341913.1:p.Tyr148His
NM_213647.3:c.442T>C MANE Select NP_998812.1:p.Tyr148His
NM_001291980.2:c.442T>C NP_001278909.1:p.Tyr148His
NM_001354984.2:c.442T>C NP_001341913.1:p.Tyr148His
NM_002011.5:c.442T>C NP_002002.3:p.Tyr148His