Canonical Allele Identifier: CA1075631933
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1741423437
gnomAD v3: 5-44359352-A-T
gnomAD v4: 5-44359352-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359352A>T , CM000667.2:g.44359352A>T GRCh38
NC_000005.9:g.44359454A>T , CM000667.1:g.44359454A>T GRCh37
NC_000005.8:g.44395211A>T NCBI36
NG_011446.1:g.34331T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+29006T>A MANE Select ENSP00000264664.4:n.325+29006T>A
ENST00000264664.4:c.325+29006T>A ENSP00000264664.4:n.325+29006T>A
NM_004465.1:c.325+29006T>A NP_004456.1:n.325+29006T>A
XM_005248264.2:c.325+29006T>A XP_005248321.1:n.325+29006T>A
XM_005248264.4:c.325+29006T>A XP_005248321.1:n.325+29006T>A
NM_004465.2:c.325+29006T>A MANE Select NP_004456.1:n.325+29006T>A
Search 100 bp 5'
Search 100 bp 3'