Canonical Allele Identifier: CA470996372

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534631C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774874C>A , CM000672.2:g.101774874C>A	GRCh38
NC_000010.10:g.103534631C>A , CM000672.1:g.103534631C>A	GRCh37
NC_000010.9:g.103524621C>A	NCBI36
NG_007151.1:g.6197G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.195G>T MANE Select	ENSP00000321797.2:p.Val65=
ENST00000618991.5:c.-118G>T	ENSP00000484420.1:n.-118G>T
ENST00000344255.8:c.162G>T	ENSP00000340039.3:p.Val54=
ENST00000320185.6:c.195G>T	ENSP00000321797.2:p.Val65=
ENST00000344255.7:c.162G>T	ENSP00000340039.3:p.Val54=
ENST00000346714.7:c.75G>T	ENSP00000344306.3:p.Val25=
ENST00000347978.2:c.108G>T	ENSP00000321945.2:p.Val36=
ENST00000469792.6:c.*159G>T	ENSP00000473299.1:n.*159G>T
ENST00000485728.1:n.71G>T
ENST00000618991.4:c.-118G>T	ENSP00000484420.1:n.-118G>T
NM_001206389.1:c.-118G>T	NP_001193318.1:n.-118G>T
NM_006119.4:c.108G>T	NP_006110.1:p.Val36=
NM_033163.3:c.195G>T	NP_149353.1:p.Val65=
NM_033164.3:c.162G>T	NP_149354.1:p.Val54=
NM_033165.3:c.75G>T	NP_149355.1:p.Val25=
XM_011539509.1:c.117G>T	XP_011537811.1:p.Val39=
NM_006119.5:c.108G>T	NP_006110.1:p.Val36=
NM_033163.4:c.195G>T	NP_149353.1:p.Val65=
NM_033164.4:c.162G>T	NP_149354.1:p.Val54=
NM_033165.4:c.75G>T	NP_149355.1:p.Val25=
NM_001206389.2:c.-118G>T	NP_001193318.1:n.-118G>T
NM_006119.6:c.108G>T	NP_006110.1:p.Val36=
NM_033163.5:c.195G>T MANE Select	NP_149353.1:p.Val65=
NM_033165.5:c.75G>T	NP_149355.1:p.Val25=