Canonical Allele Identifier: CA1543088028
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1740835130

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335812C>A , CM000667.2:g.44335812C>A GRCh38
NC_000005.9:g.44335914C>A , CM000667.1:g.44335914C>A GRCh37
NC_000005.8:g.44371671C>A NCBI36
NG_011446.1:g.57871G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25282G>T MANE Select ENSP00000264664.4:n.326-25282G>T
ENST00000264664.4:c.326-25282G>T ENSP00000264664.4:n.326-25282G>T
NM_004465.1:c.326-25282G>T NP_004456.1:n.326-25282G>T
XM_005248264.2:c.326-25282G>T XP_005248321.1:n.326-25282G>T
XM_005248264.4:c.326-25282G>T XP_005248321.1:n.326-25282G>T
NM_004465.2:c.326-25282G>T MANE Select NP_004456.1:n.326-25282G>T