Canonical Allele Identifier: CA2610620885

Gene: FGF8

Linked Data

• gnomAD v4: 10-101775526-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101775526T>C , CM000672.2:g.101775526T>C	GRCh38
NC_000010.10:g.103535283T>C , CM000672.1:g.103535283T>C	GRCh37
NC_000010.9:g.103525273T>C	NCBI36
NG_007151.1:g.5545A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.69+214A>G MANE Select	ENSP00000321797.2:n.69+214A>G
ENST00000618991.5:c.-124+214A>G	ENSP00000484420.1:n.-124+214A>G
ENST00000344255.8:c.69+214A>G	ENSP00000340039.3:n.69+214A>G
ENST00000320185.6:c.69+214A>G	ENSP00000321797.2:n.69+214A>G
ENST00000344255.7:c.69+214A>G	ENSP00000340039.3:n.69+214A>G
ENST00000346714.7:c.69+214A>G	ENSP00000344306.3:n.69+214A>G
ENST00000347978.2:c.69+214A>G	ENSP00000321945.2:n.69+214A>G
ENST00000469792.6:c.*153+16A>G	ENSP00000473299.1:n.*153+16A>G
ENST00000485728.1:n.32+343A>G
ENST00000618991.4:c.-124+214A>G	ENSP00000484420.1:n.-124+214A>G
NM_001206389.1:c.-124+214A>G	NP_001193318.1:n.-124+214A>G
NM_006119.4:c.69+214A>G	NP_006110.1:n.69+214A>G
NM_033163.3:c.69+214A>G	NP_149353.1:n.69+214A>G
NM_033164.3:c.69+214A>G	NP_149354.1:n.69+214A>G
NM_033165.3:c.69+214A>G	NP_149355.1:n.69+214A>G
XM_011539509.1:c.78+214A>G	XP_011537811.1:n.78+214A>G
NM_006119.5:c.69+214A>G	NP_006110.1:n.69+214A>G
NM_033163.4:c.69+214A>G	NP_149353.1:n.69+214A>G
NM_033164.4:c.69+214A>G	NP_149354.1:n.69+214A>G
NM_033165.4:c.69+214A>G	NP_149355.1:n.69+214A>G
NM_001206389.2:c.-124+214A>G	NP_001193318.1:n.-124+214A>G
NM_006119.6:c.69+214A>G	NP_006110.1:n.69+214A>G
NM_033163.5:c.69+214A>G MANE Select	NP_149353.1:n.69+214A>G
NM_033165.5:c.69+214A>G	NP_149355.1:n.69+214A>G