Canonical Allele Identifier: CA377836428

Gene: FGF8

Linked Data

• gnomAD v4: 10-101774784-C-A
• MyVariant Identifiers: chr10:g.103534541C>A (hg19) ; chr10:g.101774784C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774784C>A , CM000672.2:g.101774784C>A	GRCh38
NC_000010.10:g.103534541C>A , CM000672.1:g.103534541C>A	GRCh37
NC_000010.9:g.103524531C>A	NCBI36
NG_007151.1:g.6287G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.285G>T MANE Select	ENSP00000321797.2:p.Gln95His
ENST00000618991.5:c.-28G>T	ENSP00000484420.1:n.-28G>T
ENST00000344255.8:c.252G>T	ENSP00000340039.3:p.Gln84His
ENST00000320185.6:c.285G>T	ENSP00000321797.2:p.Gln95His
ENST00000344255.7:c.252G>T	ENSP00000340039.3:p.Gln84His
ENST00000346714.7:c.165G>T	ENSP00000344306.3:p.Gln55His
ENST00000347978.2:c.198G>T	ENSP00000321945.2:p.Gln66His
ENST00000469792.6:c.*249G>T	ENSP00000473299.1:n.*249G>T
ENST00000485728.1:n.161G>T
ENST00000618991.4:c.-28G>T	ENSP00000484420.1:n.-28G>T
NM_001206389.1:c.-28G>T	NP_001193318.1:n.-28G>T
NM_006119.4:c.198G>T	NP_006110.1:p.Gln66His
NM_033163.3:c.285G>T	NP_149353.1:p.Gln95His
NM_033164.3:c.252G>T	NP_149354.1:p.Gln84His
NM_033165.3:c.165G>T	NP_149355.1:p.Gln55His
XM_011539509.1:c.207G>T	XP_011537811.1:p.Gln69His
NM_006119.5:c.198G>T	NP_006110.1:p.Gln66His
NM_033163.4:c.285G>T	NP_149353.1:p.Gln95His
NM_033164.4:c.252G>T	NP_149354.1:p.Gln84His
NM_033165.4:c.165G>T	NP_149355.1:p.Gln55His
NM_001206389.2:c.-28G>T	NP_001193318.1:n.-28G>T
NM_006119.6:c.198G>T	NP_006110.1:p.Gln66His
NM_033163.5:c.285G>T MANE Select	NP_149353.1:p.Gln95His
NM_033165.5:c.165G>T	NP_149355.1:p.Gln55His