Canonical Allele Identifier: CA359697841
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1409489572
gnomAD v2: 5-44305260-C-T
gnomAD v3: 5-44305158-C-T
gnomAD v4: 5-44305158-C-T
MyVariant Identifiers: chr5:g.44305260C>T (hg19) chr5:g.44305158C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305158C>T , CM000667.2:g.44305158C>T GRCh38
NC_000005.9:g.44305260C>T , CM000667.1:g.44305260C>T GRCh37
NC_000005.8:g.44341017C>T NCBI36
NG_011446.1:g.88525G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.464G>A MANE Select ENSP00000264664.4:p.Arg155Lys
ENST00000264664.4:c.464G>A ENSP00000264664.4:p.Arg155Lys
NM_004465.1:c.464G>A NP_004456.1:p.Arg155Lys
XM_005248264.2:c.464G>A XP_005248321.1:p.Arg155Lys
XM_005248264.4:c.464G>A XP_005248321.1:p.Arg155Lys
NM_004465.2:c.464G>A MANE Select NP_004456.1:p.Arg155Lys
Search 100 bp 5'
Search 100 bp 3'