Canonical Allele Identifier: CA2708860563
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs2111773009

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335644G>A , CM000667.2:g.44335644G>A GRCh38
NC_000005.9:g.44335746G>A , CM000667.1:g.44335746G>A GRCh37
NC_000005.8:g.44371503G>A NCBI36
NG_011446.1:g.58039C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25114C>T MANE Select ENSP00000264664.4:n.326-25114C>T
ENST00000264664.4:c.326-25114C>T ENSP00000264664.4:n.326-25114C>T
NM_004465.1:c.326-25114C>T NP_004456.1:n.326-25114C>T
XM_005248264.2:c.326-25114C>T XP_005248321.1:n.326-25114C>T
XM_005248264.4:c.326-25114C>T XP_005248321.1:n.326-25114C>T
NM_004465.2:c.326-25114C>T MANE Select NP_004456.1:n.326-25114C>T