Canonical Allele Identifier: CA377836566

Gene: FGF8

Linked Data

• gnomAD v4: 10-101774792-G-T
• MyVariant Identifiers: chr10:g.103534549G>T (hg19) ; chr10:g.101774792G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774792G>T , CM000672.2:g.101774792G>T	GRCh38
NC_000010.10:g.103534549G>T , CM000672.1:g.103534549G>T	GRCh37
NC_000010.9:g.103524539G>T	NCBI36
NG_007151.1:g.6279C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.277C>A MANE Select	ENSP00000321797.2:p.His93Asn
ENST00000618991.5:c.-36C>A	ENSP00000484420.1:n.-36C>A
ENST00000344255.8:c.244C>A	ENSP00000340039.3:p.His82Asn
ENST00000320185.6:c.277C>A	ENSP00000321797.2:p.His93Asn
ENST00000344255.7:c.244C>A	ENSP00000340039.3:p.His82Asn
ENST00000346714.7:c.157C>A	ENSP00000344306.3:p.His53Asn
ENST00000347978.2:c.190C>A	ENSP00000321945.2:p.His64Asn
ENST00000469792.6:c.*241C>A	ENSP00000473299.1:n.*241C>A
ENST00000485728.1:n.153C>A
ENST00000618991.4:c.-36C>A	ENSP00000484420.1:n.-36C>A
NM_001206389.1:c.-36C>A	NP_001193318.1:n.-36C>A
NM_006119.4:c.190C>A	NP_006110.1:p.His64Asn
NM_033163.3:c.277C>A	NP_149353.1:p.His93Asn
NM_033164.3:c.244C>A	NP_149354.1:p.His82Asn
NM_033165.3:c.157C>A	NP_149355.1:p.His53Asn
XM_011539509.1:c.199C>A	XP_011537811.1:p.His67Asn
NM_006119.5:c.190C>A	NP_006110.1:p.His64Asn
NM_033163.4:c.277C>A	NP_149353.1:p.His93Asn
NM_033164.4:c.244C>A	NP_149354.1:p.His82Asn
NM_033165.4:c.157C>A	NP_149355.1:p.His53Asn
NM_001206389.2:c.-36C>A	NP_001193318.1:n.-36C>A
NM_006119.6:c.190C>A	NP_006110.1:p.His64Asn
NM_033163.5:c.277C>A MANE Select	NP_149353.1:p.His93Asn
NM_033165.5:c.157C>A	NP_149355.1:p.His53Asn