Canonical Allele Identifier: CA3576751

Gene: FGFR4

Linked Data

• dbSNP Id: rs775531357
• ExAC: 5:176524439 C / T
• gnomAD v2: 5-176524439-C-T
• gnomAD v4: 5-177097438-C-T
• MyVariant Identifiers: chr5:g.176524439C>T (hg19) ; chr5:g.177097438C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097438C>T , CM000667.2:g.177097438C>T	GRCh38
NC_000005.9:g.176524439C>T , CM000667.1:g.176524439C>T	GRCh37
NC_000005.8:g.176457045C>T	NCBI36
NG_012067.1:g.15519C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2259+41C>T MANE Select	ENSP00000292408.4:n.2259+41C>T
ENST00000292408.8:c.2259+41C>T	ENSP00000292408.4:n.2259+41C>T
ENST00000393637.5:c.2139+41C>T	ENSP00000377254.1:n.2139+41C>T
ENST00000393648.6:c.2055+41C>T	ENSP00000377259.2:n.2055+41C>T
ENST00000502906.5:c.2259+41C>T	ENSP00000424960.1:n.2259+41C>T
ENST00000513423.1:n.207+41C>T
NM_001291980.1:c.2055+41C>T	NP_001278909.1:n.2055+41C>T
NM_002011.4:c.2259+41C>T	NP_002002.3:n.2259+41C>T
NM_022963.3:c.2139+41C>T	NP_075252.2:n.2139+41C>T
NM_213647.2:c.2259+41C>T	NP_998812.1:n.2259+41C>T
XM_005265838.2:c.2259+41C>T	XP_005265895.1:n.2259+41C>T
XM_011534464.1:c.2352+41C>T	XP_011532766.1:n.2352+41C>T
XM_011534465.1:c.1941+41C>T	XP_011532767.1:n.1941+41C>T
NM_001354984.1:c.2259+41C>T	NP_001341913.1:n.2259+41C>T
NM_213647.3:c.2259+41C>T MANE Select	NP_998812.1:n.2259+41C>T
NM_001291980.2:c.2055+41C>T	NP_001278909.1:n.2055+41C>T
NM_001354984.2:c.2259+41C>T	NP_001341913.1:n.2259+41C>T
NM_002011.5:c.2259+41C>T	NP_002002.3:n.2259+41C>T