Canonical Allele Identifier: CA359698978
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388365G>C , CM000667.2:g.44388365G>C GRCh38
NC_000005.9:g.44388467G>C , CM000667.1:g.44388467G>C GRCh37
NC_000005.8:g.44424224G>C NCBI36
NG_011446.1:g.5318C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.318C>G MANE Select ENSP00000264664.4:p.Cys106Trp
ENST00000264664.4:c.318C>G ENSP00000264664.4:p.Cys106Trp
NM_004465.1:c.318C>G NP_004456.1:p.Cys106Trp
XM_005248264.2:c.318C>G XP_005248321.1:p.Cys106Trp
XM_005248264.4:c.318C>G XP_005248321.1:p.Cys106Trp
NM_004465.2:c.318C>G MANE Select NP_004456.1:p.Cys106Trp