Canonical Allele Identifier: CA359697913
Gene: FGF10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.44305288A>C (hg19) chr5:g.44305186A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305186A>C , CM000667.2:g.44305186A>C GRCh38
NC_000005.9:g.44305288A>C , CM000667.1:g.44305288A>C GRCh37
NC_000005.8:g.44341045A>C NCBI36
NG_011446.1:g.88497T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.436T>G MANE Select ENSP00000264664.4:p.Phe146Val
ENST00000264664.4:c.436T>G ENSP00000264664.4:p.Phe146Val
NM_004465.1:c.436T>G NP_004456.1:p.Phe146Val
XM_005248264.2:c.436T>G XP_005248321.1:p.Phe146Val
XM_005248264.4:c.436T>G XP_005248321.1:p.Phe146Val
NM_004465.2:c.436T>G MANE Select NP_004456.1:p.Phe146Val
Search 100 bp 5'
Search 100 bp 3'