Canonical Allele Identifier: CA118872
Gene: FGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7534
dbSNP Id: rs104893888

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388443T>G , CM000667.2:g.44388443T>G GRCh38
NC_000005.9:g.44388545T>G , CM000667.1:g.44388545T>G GRCh37
NC_000005.8:g.44424302T>G NCBI36
NG_011446.1:g.5240A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.240A>C MANE Select ENSP00000264664.4:p.Arg80Ser
ENST00000264664.4:c.240A>C ENSP00000264664.4:p.Arg80Ser
NM_004465.1:n.240A>C NP_004456.1:p.Arg80Ser
XM_005248264.2:c.240A>C XP_005248321.1:p.Arg80Ser
XM_005248264.4:c.240A>C XP_005248321.1:p.Arg80Ser
NM_004465.2:c.240A>C MANE Select NP_004456.1:p.Arg80Ser