Canonical Allele Identifier: CA3576729

Gene: FGFR4

Linked Data

• dbSNP Id: rs369140321
• ExAC: 5:176524347 C / T
• gnomAD v2: 5-176524347-C-T
• gnomAD v3: 5-177097346-C-T
• gnomAD v4: 5-177097346-C-T
• MyVariant Identifiers: chr5:g.176524347C>T (hg19) ; chr5:g.177097346C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097346C>T , CM000667.2:g.177097346C>T	GRCh38
NC_000005.9:g.176524347C>T , CM000667.1:g.176524347C>T	GRCh37
NC_000005.8:g.176456953C>T	NCBI36
NG_012067.1:g.15427C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2208C>T MANE Select	ENSP00000292408.4:p.Phe736=
ENST00000292408.8:c.2208C>T	ENSP00000292408.4:p.Phe736=
ENST00000393637.5:c.2088C>T	ENSP00000377254.1:p.Phe696=
ENST00000393648.6:c.2004C>T	ENSP00000377259.2:p.Phe668=
ENST00000502906.5:c.2208C>T	ENSP00000424960.1:p.Phe736=
ENST00000513423.1:n.156C>T
NM_001291980.1:c.2004C>T	NP_001278909.1:p.Phe668=
NM_002011.4:c.2208C>T	NP_002002.3:p.Phe736=
NM_022963.3:c.2088C>T	NP_075252.2:p.Phe696=
NM_213647.2:c.2208C>T	NP_998812.1:p.Phe736=
XM_005265838.2:c.2208C>T	XP_005265895.1:p.Phe736=
XM_011534464.1:c.2301C>T	XP_011532766.1:p.Phe767=
XM_011534465.1:c.1890C>T	XP_011532767.1:p.Phe630=
NM_001354984.1:c.2208C>T	NP_001341913.1:p.Phe736=
NM_213647.3:c.2208C>T MANE Select	NP_998812.1:p.Phe736=
NM_001291980.2:c.2004C>T	NP_001278909.1:p.Phe668=
NM_001354984.2:c.2208C>T	NP_001341913.1:p.Phe736=
NM_002011.5:c.2208C>T	NP_002002.3:p.Phe736=