Canonical Allele Identifier: CA3258534
Gene: FGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1598837
ClinVar RCV Id: RCV002122826
dbSNP Id: rs145059362
ExAC: 5:44388445 G / T
gnomAD v2: 5-44388445-G-T
gnomAD v3: 5-44388343-G-T
gnomAD v4: 5-44388343-G-T
MyVariant Identifiers: chr5:g.44388445G>T (hg19) chr5:g.44388343G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388343G>T , CM000667.2:g.44388343G>T GRCh38
NC_000005.9:g.44388445G>T , CM000667.1:g.44388445G>T GRCh37
NC_000005.8:g.44424202G>T NCBI36
NG_011446.1:g.5340C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+15C>A MANE Select ENSP00000264664.4:n.325+15C>A
ENST00000264664.4:c.325+15C>A ENSP00000264664.4:n.325+15C>A
NM_004465.1:c.325+15C>A NP_004456.1:n.325+15C>A
XM_005248264.2:c.325+15C>A XP_005248321.1:n.325+15C>A
XM_005248264.4:c.325+15C>A XP_005248321.1:n.325+15C>A
NM_004465.2:c.325+15C>A MANE Select NP_004456.1:n.325+15C>A
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