Canonical Allele Identifier: CA359699111
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1742158663
gnomAD v4: 5-44388392-C-A
MyVariant Identifiers: chr5:g.44388494C>A (hg19) chr5:g.44388392C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388392C>A , CM000667.2:g.44388392C>A GRCh38
NC_000005.9:g.44388494C>A , CM000667.1:g.44388494C>A GRCh37
NC_000005.8:g.44424251C>A NCBI36
NG_011446.1:g.5291G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.291G>T MANE Select ENSP00000264664.4:p.Lys97Asn
ENST00000264664.4:c.291G>T ENSP00000264664.4:p.Lys97Asn
NM_004465.1:c.291G>T NP_004456.1:p.Lys97Asn
XM_005248264.2:c.291G>T XP_005248321.1:p.Lys97Asn
XM_005248264.4:c.291G>T XP_005248321.1:p.Lys97Asn
NM_004465.2:c.291G>T MANE Select NP_004456.1:p.Lys97Asn
Search 100 bp 5'
Search 100 bp 3'