Canonical Allele Identifier: CA470996347

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534607A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774850A>G , CM000672.2:g.101774850A>G	GRCh38
NC_000010.10:g.103534607A>G , CM000672.1:g.103534607A>G	GRCh37
NC_000010.9:g.103524597A>G	NCBI36
NG_007151.1:g.6221T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.219T>C MANE Select	ENSP00000321797.2:p.Asp73=
ENST00000618991.5:c.-94T>C	ENSP00000484420.1:n.-94T>C
ENST00000344255.8:c.186T>C	ENSP00000340039.3:p.Asp62=
ENST00000320185.6:c.219T>C	ENSP00000321797.2:p.Asp73=
ENST00000344255.7:c.186T>C	ENSP00000340039.3:p.Asp62=
ENST00000346714.7:c.99T>C	ENSP00000344306.3:p.Asp33=
ENST00000347978.2:c.132T>C	ENSP00000321945.2:p.Asp44=
ENST00000469792.6:c.*183T>C	ENSP00000473299.1:n.*183T>C
ENST00000485728.1:n.95T>C
ENST00000618991.4:c.-94T>C	ENSP00000484420.1:n.-94T>C
NM_001206389.1:c.-94T>C	NP_001193318.1:n.-94T>C
NM_006119.4:c.132T>C	NP_006110.1:p.Asp44=
NM_033163.3:c.219T>C	NP_149353.1:p.Asp73=
NM_033164.3:c.186T>C	NP_149354.1:p.Asp62=
NM_033165.3:c.99T>C	NP_149355.1:p.Asp33=
XM_011539509.1:c.141T>C	XP_011537811.1:p.Asp47=
NM_006119.5:c.132T>C	NP_006110.1:p.Asp44=
NM_033163.4:c.219T>C	NP_149353.1:p.Asp73=
NM_033164.4:c.186T>C	NP_149354.1:p.Asp62=
NM_033165.4:c.99T>C	NP_149355.1:p.Asp33=
NM_001206389.2:c.-94T>C	NP_001193318.1:n.-94T>C
NM_006119.6:c.132T>C	NP_006110.1:p.Asp44=
NM_033163.5:c.219T>C MANE Select	NP_149353.1:p.Asp73=
NM_033165.5:c.99T>C	NP_149355.1:p.Asp33=