Canonical Allele Identifier: CA1543079847
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1740049127
gnomAD v4: 5-44305250-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305250A>T , CM000667.2:g.44305250A>T GRCh38
NC_000005.9:g.44305352A>T , CM000667.1:g.44305352A>T GRCh37
NC_000005.8:g.44341109A>T NCBI36
NG_011446.1:g.88433T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-58T>A MANE Select ENSP00000264664.4:n.430-58T>A
ENST00000264664.4:c.430-58T>A ENSP00000264664.4:n.430-58T>A
NM_004465.1:c.430-58T>A NP_004456.1:n.430-58T>A
XM_005248264.2:c.430-58T>A XP_005248321.1:n.430-58T>A
XM_005248264.4:c.430-58T>A XP_005248321.1:n.430-58T>A
NM_004465.2:c.430-58T>A MANE Select NP_004456.1:n.430-58T>A
Search 100 bp 5'
Search 100 bp 3'