Canonical Allele Identifier: CA2610620787

Gene: FGF8

Linked Data

• gnomAD v4: 10-101775443-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101775443T>G , CM000672.2:g.101775443T>G	GRCh38
NC_000010.10:g.103535200T>G , CM000672.1:g.103535200T>G	GRCh37
NC_000010.9:g.103525190T>G	NCBI36
NG_007151.1:g.5628A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.70-227A>C MANE Select	ENSP00000321797.2:n.70-227A>C
ENST00000618991.5:c.-124+297A>C	ENSP00000484420.1:n.-124+297A>C
ENST00000344255.8:c.70-227A>C	ENSP00000340039.3:n.70-227A>C
ENST00000320185.6:c.70-227A>C	ENSP00000321797.2:n.70-227A>C
ENST00000344255.7:c.70-227A>C	ENSP00000340039.3:n.70-227A>C
ENST00000346714.7:c.69+297A>C	ENSP00000344306.3:n.69+297A>C
ENST00000347978.2:c.69+297A>C	ENSP00000321945.2:n.69+297A>C
ENST00000469792.6:c.*153+99A>C	ENSP00000473299.1:n.*153+99A>C
ENST00000485728.1:n.32+426A>C
ENST00000618991.4:c.-124+297A>C	ENSP00000484420.1:n.-124+297A>C
NM_001206389.1:c.-124+297A>C	NP_001193318.1:n.-124+297A>C
NM_006119.4:c.69+297A>C	NP_006110.1:n.69+297A>C
NM_033163.3:c.70-227A>C	NP_149353.1:n.70-227A>C
NM_033164.3:c.70-227A>C	NP_149354.1:n.70-227A>C
NM_033165.3:c.69+297A>C	NP_149355.1:n.69+297A>C
XM_011539509.1:c.78+297A>C	XP_011537811.1:n.78+297A>C
NM_006119.5:c.69+297A>C	NP_006110.1:n.69+297A>C
NM_033163.4:c.70-227A>C	NP_149353.1:n.70-227A>C
NM_033164.4:c.70-227A>C	NP_149354.1:n.70-227A>C
NM_033165.4:c.69+297A>C	NP_149355.1:n.69+297A>C
NM_001206389.2:c.-124+297A>C	NP_001193318.1:n.-124+297A>C
NM_006119.6:c.69+297A>C	NP_006110.1:n.69+297A>C
NM_033163.5:c.70-227A>C MANE Select	NP_149353.1:n.70-227A>C
NM_033165.5:c.69+297A>C	NP_149355.1:n.69+297A>C