Canonical Allele Identifier: CA447724533

Gene: FGFR4

Linked Data

• dbSNP Id: rs1333763766
• MyVariant Identifiers: chr5:g.176518006C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091005C>G , CM000667.2:g.177091005C>G	GRCh38
NC_000005.9:g.176518006C>G , CM000667.1:g.176518006C>G	GRCh37
NC_000005.8:g.176450612C>G	NCBI36
NG_012067.1:g.9086C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.504C>G MANE Select	ENSP00000292408.4:p.Val168=
ENST00000292408.8:c.504C>G	ENSP00000292408.4:p.Val168=
ENST00000393637.5:c.504C>G	ENSP00000377254.1:p.Val168=
ENST00000393648.6:c.504C>G	ENSP00000377259.2:p.Val168=
ENST00000426612.5:n.621C>G
ENST00000430285.5:c.*368C>G	ENSP00000395164.1:n.*368C>G
ENST00000502906.5:c.504C>G	ENSP00000424960.1:p.Val168=
ENST00000503708.5:c.504C>G	ENSP00000424905.1:p.Val168=
ENST00000509511.5:n.504C>G
NM_001291980.1:c.504C>G	NP_001278909.1:p.Val168=
NM_002011.4:c.504C>G	NP_002002.3:p.Val168=
NM_022963.3:c.504C>G	NP_075252.2:p.Val168=
NM_213647.2:c.504C>G	NP_998812.1:p.Val168=
XM_005265838.2:c.504C>G	XP_005265895.1:p.Val168=
XM_011534464.1:c.597C>G	XP_011532766.1:p.Val199=
XM_011534465.1:c.186C>G	XP_011532767.1:p.Val62=
XR_941090.1:n.549C>G
NM_001354984.1:c.504C>G	NP_001341913.1:p.Val168=
NM_213647.3:c.504C>G MANE Select	NP_998812.1:p.Val168=
NM_001291980.2:c.504C>G	NP_001278909.1:p.Val168=
NM_001354984.2:c.504C>G	NP_001341913.1:p.Val168=
NM_002011.5:c.504C>G	NP_002002.3:p.Val168=