Canonical Allele Identifier: CA377836493
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774788A>C , CM000672.2:g.101774788A>C GRCh38
NC_000010.10:g.103534545A>C , CM000672.1:g.103534545A>C GRCh37
NC_000010.9:g.103524535A>C NCBI36
NG_007151.1:g.6283T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320185.7:c.281T>G MANE Select ENSP00000321797.2:p.Val94Gly
ENST00000618991.5:c.-32T>G ENSP00000484420.1:n.-32T>G
ENST00000344255.8:c.248T>G ENSP00000340039.3:p.Val83Gly
ENST00000320185.6:c.281T>G ENSP00000321797.2:p.Val94Gly
ENST00000344255.7:c.248T>G ENSP00000340039.3:p.Val83Gly
ENST00000346714.7:c.161T>G ENSP00000344306.3:p.Val54Gly
ENST00000347978.2:c.194T>G ENSP00000321945.2:p.Val65Gly
ENST00000469792.6:c.*245T>G ENSP00000473299.1:n.*245T>G
ENST00000485728.1:n.157T>G
ENST00000618991.4:c.-32T>G ENSP00000484420.1:n.-32T>G
NM_001206389.1:c.-32T>G NP_001193318.1:n.-32T>G
NM_006119.4:c.194T>G NP_006110.1:p.Val65Gly
NM_033163.3:c.281T>G NP_149353.1:p.Val94Gly
NM_033164.3:c.248T>G NP_149354.1:p.Val83Gly
NM_033165.3:c.161T>G NP_149355.1:p.Val54Gly
XM_011539509.1:c.203T>G XP_011537811.1:p.Val68Gly
NM_006119.5:c.194T>G NP_006110.1:p.Val65Gly
NM_033163.4:c.281T>G NP_149353.1:p.Val94Gly
NM_033164.4:c.248T>G NP_149354.1:p.Val83Gly
NM_033165.4:c.161T>G NP_149355.1:p.Val54Gly
NM_001206389.2:c.-32T>G NP_001193318.1:n.-32T>G
NM_006119.6:c.194T>G NP_006110.1:p.Val65Gly
NM_033163.5:c.281T>G MANE Select NP_149353.1:p.Val94Gly
NM_033165.5:c.161T>G NP_149355.1:p.Val54Gly