Canonical Allele Identifier: CA595189254

Gene: FGF8

Linked Data

• dbSNP Id: rs1290911120
• gnomAD v2: 10-103531366-T-G
• gnomAD v4: 10-101771609-T-G
• MyVariant Identifiers: chr10:g.103531366T>G (hg19) ; chr10:g.101771609T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771609T>G , CM000672.2:g.101771609T>G	GRCh38
NC_000010.10:g.103531366T>G , CM000672.1:g.103531366T>G	GRCh37
NC_000010.9:g.103521356T>G	NCBI36
NG_007151.1:g.9462A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.338-40A>C MANE Select	ENSP00000321797.2:n.338-40A>C
ENST00000618991.5:c.26-40A>C	ENSP00000484420.1:n.26-40A>C
ENST00000344255.8:c.305-40A>C	ENSP00000340039.3:n.305-40A>C
ENST00000320185.6:c.338-40A>C	ENSP00000321797.2:n.338-40A>C
ENST00000344255.7:c.305-40A>C	ENSP00000340039.3:n.305-40A>C
ENST00000346714.7:c.218-40A>C	ENSP00000344306.3:n.218-40A>C
ENST00000347978.2:c.251-40A>C	ENSP00000321945.2:n.251-40A>C
ENST00000469792.6:c.*302-40A>C	ENSP00000473299.1:n.*302-40A>C
ENST00000485728.1:n.214-40A>C
ENST00000618991.4:c.26-40A>C	ENSP00000484420.1:n.26-40A>C
NM_001206389.1:c.26-40A>C	NP_001193318.1:n.26-40A>C
NM_006119.4:c.251-40A>C	NP_006110.1:n.251-40A>C
NM_033163.3:c.338-40A>C	NP_149353.1:n.338-40A>C
NM_033164.3:c.305-40A>C	NP_149354.1:n.305-40A>C
NM_033165.3:c.218-40A>C	NP_149355.1:n.218-40A>C
XM_011539509.1:c.260-40A>C	XP_011537811.1:n.260-40A>C
XR_946252.2:n.411T>G
XR_946253.2:n.409T>G
NM_006119.5:c.251-40A>C	NP_006110.1:n.251-40A>C
NM_033163.4:c.338-40A>C	NP_149353.1:n.338-40A>C
NM_033164.4:c.305-40A>C	NP_149354.1:n.305-40A>C
NM_033165.4:c.218-40A>C	NP_149355.1:n.218-40A>C
NM_001206389.2:c.26-40A>C	NP_001193318.1:n.26-40A>C
NM_006119.6:c.251-40A>C	NP_006110.1:n.251-40A>C
NM_033163.5:c.338-40A>C MANE Select	NP_149353.1:n.338-40A>C
NM_033165.5:c.218-40A>C	NP_149355.1:n.218-40A>C