Canonical Allele Identifier: CA2673772752
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs2111667599
gnomAD v4: 5-44305249-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305249G>A , CM000667.2:g.44305249G>A GRCh38
NC_000005.9:g.44305351G>A , CM000667.1:g.44305351G>A GRCh37
NC_000005.8:g.44341108G>A NCBI36
NG_011446.1:g.88434C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-57C>T MANE Select ENSP00000264664.4:n.430-57C>T
ENST00000264664.4:c.430-57C>T ENSP00000264664.4:n.430-57C>T
NM_004465.1:c.430-57C>T NP_004456.1:n.430-57C>T
XM_005248264.2:c.430-57C>T XP_005248321.1:n.430-57C>T
XM_005248264.4:c.430-57C>T XP_005248321.1:n.430-57C>T
NM_004465.2:c.430-57C>T MANE Select NP_004456.1:n.430-57C>T
Search 100 bp 5'
Search 100 bp 3'