Canonical Allele Identifier: CA470996383

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534640T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774883T>G , CM000672.2:g.101774883T>G	GRCh38
NC_000010.10:g.103534640T>G , CM000672.1:g.103534640T>G	GRCh37
NC_000010.9:g.103524630T>G	NCBI36
NG_007151.1:g.6188A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.186A>C MANE Select	ENSP00000321797.2:p.Thr62=
ENST00000618991.5:c.-123-4A>C	ENSP00000484420.1:n.-123-4A>C
ENST00000344255.8:c.157-4A>C	ENSP00000340039.3:n.157-4A>C
ENST00000320185.6:c.186A>C	ENSP00000321797.2:p.Thr62=
ENST00000344255.7:c.157-4A>C	ENSP00000340039.3:n.157-4A>C
ENST00000346714.7:c.70-4A>C	ENSP00000344306.3:n.70-4A>C
ENST00000347978.2:c.99A>C	ENSP00000321945.2:p.Thr33=
ENST00000469792.6:c.*154-4A>C	ENSP00000473299.1:n.*154-4A>C
ENST00000485728.1:n.62A>C
ENST00000618991.4:c.-123-4A>C	ENSP00000484420.1:n.-123-4A>C
NM_001206389.1:c.-123-4A>C	NP_001193318.1:n.-123-4A>C
NM_006119.4:c.99A>C	NP_006110.1:p.Thr33=
NM_033163.3:c.186A>C	NP_149353.1:p.Thr62=
NM_033164.3:c.157-4A>C	NP_149354.1:n.157-4A>C
NM_033165.3:c.70-4A>C	NP_149355.1:n.70-4A>C
XM_011539509.1:c.108A>C	XP_011537811.1:p.Thr36=
NM_006119.5:c.99A>C	NP_006110.1:p.Thr33=
NM_033163.4:c.186A>C	NP_149353.1:p.Thr62=
NM_033164.4:c.157-4A>C	NP_149354.1:n.157-4A>C
NM_033165.4:c.70-4A>C	NP_149355.1:n.70-4A>C
NM_001206389.2:c.-123-4A>C	NP_001193318.1:n.-123-4A>C
NM_006119.6:c.99A>C	NP_006110.1:p.Thr33=
NM_033163.5:c.186A>C MANE Select	NP_149353.1:p.Thr62=
NM_033165.5:c.70-4A>C	NP_149355.1:n.70-4A>C