Canonical Allele Identifier: CA3258497
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs200054156
ExAC: 5:44305326 A / C
gnomAD v2: 5-44305326-A-C
MyVariant Identifiers: chr5:g.44305326A>C (hg19) chr5:g.44305224A>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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