Canonical Allele Identifier: CA359699426
Gene: FGF10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.44388567A>T (hg19) chr5:g.44388465A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388465A>T , CM000667.2:g.44388465A>T GRCh38
NC_000005.9:g.44388567A>T , CM000667.1:g.44388567A>T GRCh37
NC_000005.8:g.44424324A>T NCBI36
NG_011446.1:g.5218T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.218T>A MANE Select ENSP00000264664.4:p.Leu73His
ENST00000264664.4:c.218T>A ENSP00000264664.4:p.Leu73His
NM_004465.1:c.218T>A NP_004456.1:p.Leu73His
XM_005248264.2:c.218T>A XP_005248321.1:p.Leu73His
XM_005248264.4:c.218T>A XP_005248321.1:p.Leu73His
NM_004465.2:c.218T>A MANE Select NP_004456.1:p.Leu73His
Search 100 bp 5'
Search 100 bp 3'