Canonical Allele Identifier: CA558949870

Gene: FGF10

Linked Data

• dbSNP Id: rs1159422797
• gnomAD v2: 5-44305686-A-T
• gnomAD v3: 5-44305584-A-T
• gnomAD v4: 5-44305584-A-T
• MyVariant Identifiers: chr5:g.44305686A>T (hg19) ; chr5:g.44305584A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305584A>T , CM000667.2:g.44305584A>T	GRCh38
NC_000005.9:g.44305686A>T , CM000667.1:g.44305686A>T	GRCh37
NC_000005.8:g.44341443A>T	NCBI36
NG_011446.1:g.88099T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.430-392T>A MANE Select	ENSP00000264664.4:n.430-392T>A
ENST00000264664.4:c.430-392T>A	ENSP00000264664.4:n.430-392T>A
NM_004465.1:c.430-392T>A	NP_004456.1:n.430-392T>A
XM_005248264.2:c.430-392T>A	XP_005248321.1:n.430-392T>A
XM_005248264.4:c.430-392T>A	XP_005248321.1:n.430-392T>A
NM_004465.2:c.430-392T>A MANE Select	NP_004456.1:n.430-392T>A