Canonical Allele Identifier: CA377837132

Gene: FGF8

Linked Data

• dbSNP Id: rs1474057032
• gnomAD v4: 10-101774854-G-A
• MyVariant Identifiers: chr10:g.103534611G>A (hg19) ; chr10:g.101774854G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774854G>A , CM000672.2:g.101774854G>A	GRCh38
NC_000010.10:g.103534611G>A , CM000672.1:g.103534611G>A	GRCh37
NC_000010.9:g.103524601G>A	NCBI36
NG_007151.1:g.6217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.215C>T MANE Select	ENSP00000321797.2:p.Thr72Met
ENST00000618991.5:c.-98C>T	ENSP00000484420.1:n.-98C>T
ENST00000344255.8:c.182C>T	ENSP00000340039.3:p.Thr61Met
ENST00000320185.6:c.215C>T	ENSP00000321797.2:p.Thr72Met
ENST00000344255.7:c.182C>T	ENSP00000340039.3:p.Thr61Met
ENST00000346714.7:c.95C>T	ENSP00000344306.3:p.Thr32Met
ENST00000347978.2:c.128C>T	ENSP00000321945.2:p.Thr43Met
ENST00000469792.6:c.*179C>T	ENSP00000473299.1:n.*179C>T
ENST00000485728.1:n.91C>T
ENST00000618991.4:c.-98C>T	ENSP00000484420.1:n.-98C>T
NM_001206389.1:c.-98C>T	NP_001193318.1:n.-98C>T
NM_006119.4:c.128C>T	NP_006110.1:p.Thr43Met
NM_033163.3:c.215C>T	NP_149353.1:p.Thr72Met
NM_033164.3:c.182C>T	NP_149354.1:p.Thr61Met
NM_033165.3:c.95C>T	NP_149355.1:p.Thr32Met
XM_011539509.1:c.137C>T	XP_011537811.1:p.Thr46Met
NM_006119.5:c.128C>T	NP_006110.1:p.Thr43Met
NM_033163.4:c.215C>T	NP_149353.1:p.Thr72Met
NM_033164.4:c.182C>T	NP_149354.1:p.Thr61Met
NM_033165.4:c.95C>T	NP_149355.1:p.Thr32Met
NM_001206389.2:c.-98C>T	NP_001193318.1:n.-98C>T
NM_006119.6:c.128C>T	NP_006110.1:p.Thr43Met
NM_033163.5:c.215C>T MANE Select	NP_149353.1:p.Thr72Met
NM_033165.5:c.95C>T	NP_149355.1:p.Thr32Met