Canonical Allele Identifier: CA2673772742
Gene: FGF10 HGNC NCBI

Linked Data

gnomAD v4: 5-44305224-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305224A>T , CM000667.2:g.44305224A>T GRCh38
NC_000005.9:g.44305326A>T , CM000667.1:g.44305326A>T GRCh37
NC_000005.8:g.44341083A>T NCBI36
NG_011446.1:g.88459T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-32T>A MANE Select ENSP00000264664.4:n.430-32T>A
ENST00000264664.4:c.430-32T>A ENSP00000264664.4:n.430-32T>A
NM_004465.1:c.430-32T>A NP_004456.1:n.430-32T>A
XM_005248264.2:c.430-32T>A XP_005248321.1:n.430-32T>A
XM_005248264.4:c.430-32T>A XP_005248321.1:n.430-32T>A
NM_004465.2:c.430-32T>A MANE Select NP_004456.1:n.430-32T>A
Search 100 bp 5'
Search 100 bp 3'