Canonical Allele Identifier: CA2610620066

Gene: FGF8

Linked Data

• gnomAD v4: 10-101771705-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771705A>G , CM000672.2:g.101771705A>G	GRCh38
NC_000010.10:g.103531462A>G , CM000672.1:g.103531462A>G	GRCh37
NC_000010.9:g.103521452A>G	NCBI36
NG_007151.1:g.9366T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.338-136T>C MANE Select	ENSP00000321797.2:n.338-136T>C
ENST00000618991.5:c.26-136T>C	ENSP00000484420.1:n.26-136T>C
ENST00000344255.8:c.305-136T>C	ENSP00000340039.3:n.305-136T>C
ENST00000320185.6:c.338-136T>C	ENSP00000321797.2:n.338-136T>C
ENST00000344255.7:c.305-136T>C	ENSP00000340039.3:n.305-136T>C
ENST00000346714.7:c.218-136T>C	ENSP00000344306.3:n.218-136T>C
ENST00000347978.2:c.251-136T>C	ENSP00000321945.2:n.251-136T>C
ENST00000469792.6:c.*302-136T>C	ENSP00000473299.1:n.*302-136T>C
ENST00000485728.1:n.214-136T>C
ENST00000618991.4:c.26-136T>C	ENSP00000484420.1:n.26-136T>C
NM_001206389.1:c.26-136T>C	NP_001193318.1:n.26-136T>C
NM_006119.4:c.251-136T>C	NP_006110.1:n.251-136T>C
NM_033163.3:c.338-136T>C	NP_149353.1:n.338-136T>C
NM_033164.3:c.305-136T>C	NP_149354.1:n.305-136T>C
NM_033165.3:c.218-136T>C	NP_149355.1:n.218-136T>C
XM_011539509.1:c.260-136T>C	XP_011537811.1:n.260-136T>C
XR_946252.2:n.507A>G
XR_946253.2:n.505A>G
NM_006119.5:c.251-136T>C	NP_006110.1:n.251-136T>C
NM_033163.4:c.338-136T>C	NP_149353.1:n.338-136T>C
NM_033164.4:c.305-136T>C	NP_149354.1:n.305-136T>C
NM_033165.4:c.218-136T>C	NP_149355.1:n.218-136T>C
NM_001206389.2:c.26-136T>C	NP_001193318.1:n.26-136T>C
NM_006119.6:c.251-136T>C	NP_006110.1:n.251-136T>C
NM_033163.5:c.338-136T>C MANE Select	NP_149353.1:n.338-136T>C
NM_033165.5:c.218-136T>C	NP_149355.1:n.218-136T>C