Canonical Allele Identifier: CA470996405

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534667T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774910T>G , CM000672.2:g.101774910T>G	GRCh38
NC_000010.10:g.103534667T>G , CM000672.1:g.103534667T>G	GRCh37
NC_000010.9:g.103524657T>G	NCBI36
NG_007151.1:g.6161A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.159A>C MANE Select	ENSP00000321797.2:p.Val53=
ENST00000618991.5:c.-123-31A>C	ENSP00000484420.1:n.-123-31A>C
ENST00000344255.8:c.157-31A>C	ENSP00000340039.3:n.157-31A>C
ENST00000320185.6:c.159A>C	ENSP00000321797.2:p.Val53=
ENST00000344255.7:c.157-31A>C	ENSP00000340039.3:n.157-31A>C
ENST00000346714.7:c.70-31A>C	ENSP00000344306.3:n.70-31A>C
ENST00000347978.2:c.72A>C	ENSP00000321945.2:p.Val24=
ENST00000469792.6:c.*154-31A>C	ENSP00000473299.1:n.*154-31A>C
ENST00000485728.1:n.35A>C
ENST00000618991.4:c.-123-31A>C	ENSP00000484420.1:n.-123-31A>C
NM_001206389.1:c.-123-31A>C	NP_001193318.1:n.-123-31A>C
NM_006119.4:c.72A>C	NP_006110.1:p.Val24=
NM_033163.3:c.159A>C	NP_149353.1:p.Val53=
NM_033164.3:c.157-31A>C	NP_149354.1:n.157-31A>C
NM_033165.3:c.70-31A>C	NP_149355.1:n.70-31A>C
XM_011539509.1:c.81A>C	XP_011537811.1:p.Val27=
NM_006119.5:c.72A>C	NP_006110.1:p.Val24=
NM_033163.4:c.159A>C	NP_149353.1:p.Val53=
NM_033164.4:c.157-31A>C	NP_149354.1:n.157-31A>C
NM_033165.4:c.70-31A>C	NP_149355.1:n.70-31A>C
NM_001206389.2:c.-123-31A>C	NP_001193318.1:n.-123-31A>C
NM_006119.6:c.72A>C	NP_006110.1:p.Val24=
NM_033163.5:c.159A>C MANE Select	NP_149353.1:p.Val53=
NM_033165.5:c.70-31A>C	NP_149355.1:n.70-31A>C