Canonical Allele Identifier: CA470996032

Gene: FGF8

Linked Data

• gnomAD v4: 10-101771499-G-A
• MyVariant Identifiers: chr10:g.103531256G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771499G>A , CM000672.2:g.101771499G>A	GRCh38
NC_000010.10:g.103531256G>A , CM000672.1:g.103531256G>A	GRCh37
NC_000010.9:g.103521246G>A	NCBI36
NG_007151.1:g.9572C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.408C>T MANE Select	ENSP00000321797.2:p.Tyr136=
ENST00000618991.5:c.96C>T	ENSP00000484420.1:p.Tyr32=
ENST00000344255.8:c.375C>T	ENSP00000340039.3:p.Tyr125=
ENST00000320185.6:c.408C>T	ENSP00000321797.2:p.Tyr136=
ENST00000344255.7:c.375C>T	ENSP00000340039.3:p.Tyr125=
ENST00000346714.7:c.288C>T	ENSP00000344306.3:p.Tyr96=
ENST00000347978.2:c.321C>T	ENSP00000321945.2:p.Tyr107=
ENST00000469792.6:c.*372C>T	ENSP00000473299.1:n.*372C>T
ENST00000485728.1:n.284C>T
ENST00000618991.4:c.96C>T	ENSP00000484420.1:p.Tyr32=
NM_001206389.1:c.96C>T	NP_001193318.1:p.Tyr32=
NM_006119.4:c.321C>T	NP_006110.1:p.Tyr107=
NM_033163.3:c.408C>T	NP_149353.1:p.Tyr136=
NM_033164.3:c.375C>T	NP_149354.1:p.Tyr125=
NM_033165.3:c.288C>T	NP_149355.1:p.Tyr96=
XM_011539509.1:c.330C>T	XP_011537811.1:p.Tyr110=
XR_946251.1:n.280G>A
XR_946252.1:n.211G>A
XR_946253.1:n.209G>A
XR_946252.2:n.301G>A
XR_946253.2:n.299G>A
NM_006119.5:c.321C>T	NP_006110.1:p.Tyr107=
NM_033163.4:c.408C>T	NP_149353.1:p.Tyr136=
NM_033164.4:c.375C>T	NP_149354.1:p.Tyr125=
NM_033165.4:c.288C>T	NP_149355.1:p.Tyr96=
NM_001206389.2:c.96C>T	NP_001193318.1:p.Tyr32=
NM_006119.6:c.321C>T	NP_006110.1:p.Tyr107=
NM_033163.5:c.408C>T MANE Select	NP_149353.1:p.Tyr136=
NM_033165.5:c.288C>T	NP_149355.1:p.Tyr96=