Canonical Allele Identifier: CA810983596
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1322974629
MyVariant Identifiers: chr5:g.44335837A>T (hg19) chr5:g.44335735A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335735A>T , CM000667.2:g.44335735A>T GRCh38
NC_000005.9:g.44335837A>T , CM000667.1:g.44335837A>T GRCh37
NC_000005.8:g.44371594A>T NCBI36
NG_011446.1:g.57948T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.326-25205T>A MANE Select ENSP00000264664.4:n.326-25205T>A
ENST00000264664.4:c.326-25205T>A ENSP00000264664.4:n.326-25205T>A
NM_004465.1:c.326-25205T>A NP_004456.1:n.326-25205T>A
XM_005248264.2:c.326-25205T>A XP_005248321.1:n.326-25205T>A
XM_005248264.4:c.326-25205T>A XP_005248321.1:n.326-25205T>A
NM_004465.2:c.326-25205T>A MANE Select NP_004456.1:n.326-25205T>A
Search 100 bp 5'
Search 100 bp 3'