Canonical Allele Identifier: CA118167649
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs339501

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365531C>T , CM000667.2:g.44365531C>T GRCh38
NC_000005.9:g.44365633C>T , CM000667.1:g.44365633C>T GRCh37
NC_000005.8:g.44401390C>T NCBI36
NG_011446.1:g.28152G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+22827G>A MANE Select ENSP00000264664.4:p.=
ENST00000264664.4:c.325+22827G>A ENSP00000264664.4:p.=
NM_004465.1:n.325+22827G>A NP_004456.1:p.=
XM_005248264.2:c.325+22827G>A XP_005248321.1:p.=
XM_005248264.4:c.325+22827G>A XP_005248321.1:p.=
NM_004465.2:c.325+22827G>A MANE Select NP_004456.1:p.=