Canonical Allele Identifier: CA359698949
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388358T>G , CM000667.2:g.44388358T>G GRCh38
NC_000005.9:g.44388460T>G , CM000667.1:g.44388460T>G GRCh37
NC_000005.8:g.44424217T>G NCBI36
NG_011446.1:g.5325A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325A>C MANE Select ENSP00000264664.4:p.Ser109Arg
ENST00000264664.4:c.325A>C ENSP00000264664.4:p.Ser109Arg
NM_004465.1:c.325A>C NP_004456.1:p.Ser109Arg
XM_005248264.2:c.325A>C XP_005248321.1:p.Ser109Arg
XM_005248264.4:c.325A>C XP_005248321.1:p.Ser109Arg
NM_004465.2:c.325A>C MANE Select NP_004456.1:p.Ser109Arg