Canonical Allele Identifier: CA3258500

Gene: FGF10

Linked Data

• dbSNP Id: rs765396280
• ExAC: 5:44305329 G / T
• gnomAD v2: 5-44305329-G-T
• gnomAD v4: 5-44305227-G-T
• MyVariant Identifiers: chr5:g.44305329G>T (hg19) ; chr5:g.44305227G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305227G>T , CM000667.2:g.44305227G>T	GRCh38
NC_000005.9:g.44305329G>T , CM000667.1:g.44305329G>T	GRCh37
NC_000005.8:g.44341086G>T	NCBI36
NG_011446.1:g.88456C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-35C>A MANE Select	ENSP00000264664.4:n.430-35C>A
ENST00000264664.4:c.430-35C>A	ENSP00000264664.4:n.430-35C>A
NM_004465.1:c.430-35C>A	NP_004456.1:n.430-35C>A
XM_005248264.2:c.430-35C>A	XP_005248321.1:n.430-35C>A
XM_005248264.4:c.430-35C>A	XP_005248321.1:n.430-35C>A
NM_004465.2:c.430-35C>A MANE Select	NP_004456.1:n.430-35C>A