Canonical Allele Identifier: CA1075628395
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1740057888
gnomAD v3: 5-44305589-A-G
gnomAD v4: 5-44305589-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305589A>G , CM000667.2:g.44305589A>G GRCh38
NC_000005.9:g.44305691A>G , CM000667.1:g.44305691A>G GRCh37
NC_000005.8:g.44341448A>G NCBI36
NG_011446.1:g.88094T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-397T>C MANE Select ENSP00000264664.4:n.430-397T>C
ENST00000264664.4:c.430-397T>C ENSP00000264664.4:n.430-397T>C
NM_004465.1:c.430-397T>C NP_004456.1:n.430-397T>C
XM_005248264.2:c.430-397T>C XP_005248321.1:n.430-397T>C
XM_005248264.4:c.430-397T>C XP_005248321.1:n.430-397T>C
NM_004465.2:c.430-397T>C MANE Select NP_004456.1:n.430-397T>C
Search 100 bp 5'
Search 100 bp 3'