Canonical Allele Identifier: CA15370080
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs2121875

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365443C>A , CM000667.2:g.44365443C>A GRCh38
NC_000005.9:g.44365545C>A , CM000667.1:g.44365545C>A GRCh37
NC_000005.8:g.44401302C>A NCBI36
NG_011446.1:g.28240G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+22915G>T MANE Select ENSP00000264664.4:p.=
ENST00000264664.4:c.325+22915G>T ENSP00000264664.4:p.=
NM_004465.1:n.325+22915G>T NP_004456.1:p.=
XM_005248264.2:c.325+22915G>T XP_005248321.1:p.=
XM_005248264.4:c.325+22915G>T XP_005248321.1:p.=
NM_004465.2:c.325+22915G>T MANE Select NP_004456.1:p.=