Canonical Allele Identifier: CA359698945

Gene: FGF10

Linked Data

• dbSNP Id: rs2111939010
• MyVariant Identifiers: chr5:g.44388459C>T (hg19) ; chr5:g.44388357C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44388357C>T , CM000667.2:g.44388357C>T	GRCh38
NC_000005.9:g.44388459C>T , CM000667.1:g.44388459C>T	GRCh37
NC_000005.8:g.44424216C>T	NCBI36
NG_011446.1:g.5326G>A

Transcript Alleles

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