Canonical Allele Identifier: CA444400484
Gene: FGF10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.44388560T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388458T>A , CM000667.2:g.44388458T>A GRCh38
NC_000005.9:g.44388560T>A , CM000667.1:g.44388560T>A GRCh37
NC_000005.8:g.44424317T>A NCBI36
NG_011446.1:g.5225A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.225A>T MANE Select ENSP00000264664.4:p.Gly75=
ENST00000264664.4:c.225A>T ENSP00000264664.4:p.Gly75=
NM_004465.1:c.225A>T NP_004456.1:p.Gly75=
XM_005248264.2:c.225A>T XP_005248321.1:p.Gly75=
XM_005248264.4:c.225A>T XP_005248321.1:p.Gly75=
NM_004465.2:c.225A>T MANE Select NP_004456.1:p.Gly75=