Canonical Allele Identifier: CA212180868

Gene: FGF8

Linked Data

• dbSNP Id: rs745920134
• gnomAD v2: 10-103531503-G-A
• gnomAD v3: 10-101771746-G-A
• gnomAD v4: 10-101771746-G-A
• MyVariant Identifiers: chr10:g.103531503G>A (hg19) ; chr10:g.101771746G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771746G>A , CM000672.2:g.101771746G>A	GRCh38
NC_000010.10:g.103531503G>A , CM000672.1:g.103531503G>A	GRCh37
NC_000010.9:g.103521493G>A	NCBI36
NG_007151.1:g.9325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.338-177C>T MANE Select	ENSP00000321797.2:n.338-177C>T
ENST00000618991.5:c.26-177C>T	ENSP00000484420.1:n.26-177C>T
ENST00000344255.8:c.305-177C>T	ENSP00000340039.3:n.305-177C>T
ENST00000320185.6:c.338-177C>T	ENSP00000321797.2:n.338-177C>T
ENST00000344255.7:c.305-177C>T	ENSP00000340039.3:n.305-177C>T
ENST00000346714.7:c.218-177C>T	ENSP00000344306.3:n.218-177C>T
ENST00000347978.2:c.251-177C>T	ENSP00000321945.2:n.251-177C>T
ENST00000469792.6:c.*302-177C>T	ENSP00000473299.1:n.*302-177C>T
ENST00000485728.1:n.214-177C>T
ENST00000618991.4:c.26-177C>T	ENSP00000484420.1:n.26-177C>T
NM_001206389.1:c.26-177C>T	NP_001193318.1:n.26-177C>T
NM_006119.4:c.251-177C>T	NP_006110.1:n.251-177C>T
NM_033163.3:c.338-177C>T	NP_149353.1:n.338-177C>T
NM_033164.3:c.305-177C>T	NP_149354.1:n.305-177C>T
NM_033165.3:c.218-177C>T	NP_149355.1:n.218-177C>T
XM_011539509.1:c.260-177C>T	XP_011537811.1:n.260-177C>T
XR_946252.2:n.548G>A
XR_946253.2:n.546G>A
NM_006119.5:c.251-177C>T	NP_006110.1:n.251-177C>T
NM_033163.4:c.338-177C>T	NP_149353.1:n.338-177C>T
NM_033164.4:c.305-177C>T	NP_149354.1:n.305-177C>T
NM_033165.4:c.218-177C>T	NP_149355.1:n.218-177C>T
NM_001206389.2:c.26-177C>T	NP_001193318.1:n.26-177C>T
NM_006119.6:c.251-177C>T	NP_006110.1:n.251-177C>T
NM_033163.5:c.338-177C>T MANE Select	NP_149353.1:n.338-177C>T
NM_033165.5:c.218-177C>T	NP_149355.1:n.218-177C>T