Canonical Allele Identifier: CA810998060
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1345879199
gnomAD v3: 5-44359413-C-T
gnomAD v4: 5-44359413-C-T
MyVariant Identifiers: chr5:g.44359515C>T (hg19) chr5:g.44359413C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359413C>T , CM000667.2:g.44359413C>T GRCh38
NC_000005.9:g.44359515C>T , CM000667.1:g.44359515C>T GRCh37
NC_000005.8:g.44395272C>T NCBI36
NG_011446.1:g.34270G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+28945G>A MANE Select ENSP00000264664.4:n.325+28945G>A
ENST00000264664.4:c.325+28945G>A ENSP00000264664.4:n.325+28945G>A
NM_004465.1:c.325+28945G>A NP_004456.1:n.325+28945G>A
XM_005248264.2:c.325+28945G>A XP_005248321.1:n.325+28945G>A
XM_005248264.4:c.325+28945G>A XP_005248321.1:n.325+28945G>A
NM_004465.2:c.325+28945G>A MANE Select NP_004456.1:n.325+28945G>A
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