Canonical Allele Identifier: CA359698954
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.323A>G MANE Select ENSP00000264664.4:p.Tyr108Cys
ENST00000264664.4:c.323A>G ENSP00000264664.4:p.Tyr108Cys
NM_004465.1:c.323A>G NP_004456.1:p.Tyr108Cys
XM_005248264.2:c.323A>G XP_005248321.1:p.Tyr108Cys
XM_005248264.4:c.323A>G XP_005248321.1:p.Tyr108Cys
NM_004465.2:c.323A>G MANE Select NP_004456.1:p.Tyr108Cys