Canonical Allele Identifier: CA359698952
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388360T>A , CM000667.2:g.44388360T>A GRCh38
NC_000005.9:g.44388462T>A , CM000667.1:g.44388462T>A GRCh37
NC_000005.8:g.44424219T>A NCBI36
NG_011446.1:g.5323A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.323A>T MANE Select ENSP00000264664.4:p.Tyr108Phe
ENST00000264664.4:c.323A>T ENSP00000264664.4:p.Tyr108Phe
NM_004465.1:c.323A>T NP_004456.1:p.Tyr108Phe
XM_005248264.2:c.323A>T XP_005248321.1:p.Tyr108Phe
XM_005248264.4:c.323A>T XP_005248321.1:p.Tyr108Phe
NM_004465.2:c.323A>T MANE Select NP_004456.1:p.Tyr108Phe