Canonical Allele Identifier: CA444230966

Gene: FGF10

Linked Data

• dbSNP Id: rs1740047416
• MyVariant Identifiers: chr5:g.44305270G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305168G>A , CM000667.2:g.44305168G>A	GRCh38
NC_000005.9:g.44305270G>A , CM000667.1:g.44305270G>A	GRCh37
NC_000005.8:g.44341027G>A	NCBI36
NG_011446.1:g.88515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.454C>T MANE Select	ENSP00000264664.4:p.Leu152=
ENST00000264664.4:c.454C>T	ENSP00000264664.4:p.Leu152=
NM_004465.1:c.454C>T	NP_004456.1:p.Leu152=
XM_005248264.2:c.454C>T	XP_005248321.1:p.Leu152=
XM_005248264.4:c.454C>T	XP_005248321.1:p.Leu152=
NM_004465.2:c.454C>T MANE Select	NP_004456.1:p.Leu152=