Canonical Allele Identifier: CA470996276

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534496G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774739G>A , CM000672.2:g.101774739G>A	GRCh38
NC_000010.10:g.103534496G>A , CM000672.1:g.103534496G>A	GRCh37
NC_000010.9:g.103524486G>A	NCBI36
NG_007151.1:g.6332C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.330C>T MANE Select	ENSP00000321797.2:p.Asp110=
ENST00000618991.5:c.18C>T	ENSP00000484420.1:p.Asp6=
ENST00000344255.8:c.297C>T	ENSP00000340039.3:p.Asp99=
ENST00000320185.6:c.330C>T	ENSP00000321797.2:p.Asp110=
ENST00000344255.7:c.297C>T	ENSP00000340039.3:p.Asp99=
ENST00000346714.7:c.210C>T	ENSP00000344306.3:p.Asp70=
ENST00000347978.2:c.243C>T	ENSP00000321945.2:p.Asp81=
ENST00000469792.6:c.*294C>T	ENSP00000473299.1:n.*294C>T
ENST00000485728.1:n.206C>T
ENST00000618991.4:c.18C>T	ENSP00000484420.1:p.Asp6=
NM_001206389.1:c.18C>T	NP_001193318.1:p.Asp6=
NM_006119.4:c.243C>T	NP_006110.1:p.Asp81=
NM_033163.3:c.330C>T	NP_149353.1:p.Asp110=
NM_033164.3:c.297C>T	NP_149354.1:p.Asp99=
NM_033165.3:c.210C>T	NP_149355.1:p.Asp70=
XM_011539509.1:c.252C>T	XP_011537811.1:p.Asp84=
NM_006119.5:c.243C>T	NP_006110.1:p.Asp81=
NM_033163.4:c.330C>T	NP_149353.1:p.Asp110=
NM_033164.4:c.297C>T	NP_149354.1:p.Asp99=
NM_033165.4:c.210C>T	NP_149355.1:p.Asp70=
NM_001206389.2:c.18C>T	NP_001193318.1:p.Asp6=
NM_006119.6:c.243C>T	NP_006110.1:p.Asp81=
NM_033163.5:c.330C>T MANE Select	NP_149353.1:p.Asp110=
NM_033165.5:c.210C>T	NP_149355.1:p.Asp70=