Canonical Allele Identifier: CA118170244
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs200701392
gnomAD v4: 5-44388363-G-C
MyVariant Identifiers: chr5:g.44388465G>C (hg19) chr5:g.44388363G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388363G>C , CM000667.2:g.44388363G>C GRCh38
NC_000005.9:g.44388465G>C , CM000667.1:g.44388465G>C GRCh37
NC_000005.8:g.44424222G>C NCBI36
NG_011446.1:g.5320C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.320C>G MANE Select ENSP00000264664.4:p.Pro107Arg
ENST00000264664.4:c.320C>G ENSP00000264664.4:p.Pro107Arg
NM_004465.1:c.320C>G NP_004456.1:p.Pro107Arg
XM_005248264.2:c.320C>G XP_005248321.1:p.Pro107Arg
XM_005248264.4:c.320C>G XP_005248321.1:p.Pro107Arg
NM_004465.2:c.320C>G MANE Select NP_004456.1:p.Pro107Arg
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