Canonical Allele Identifier: CA559293712

Gene: FGF10

Linked Data

• dbSNP Id: rs1414133148
• gnomAD v2: 5-44305417-G-A
• gnomAD v4: 5-44305315-G-A
• MyVariant Identifiers: chr5:g.44305417G>A (hg19) ; chr5:g.44305315G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305315G>A , CM000667.2:g.44305315G>A	GRCh38
NC_000005.9:g.44305417G>A , CM000667.1:g.44305417G>A	GRCh37
NC_000005.8:g.44341174G>A	NCBI36
NG_011446.1:g.88368C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-123C>T MANE Select	ENSP00000264664.4:n.430-123C>T
ENST00000264664.4:c.430-123C>T	ENSP00000264664.4:n.430-123C>T
NM_004465.1:c.430-123C>T	NP_004456.1:n.430-123C>T
XM_005248264.2:c.430-123C>T	XP_005248321.1:n.430-123C>T
XM_005248264.4:c.430-123C>T	XP_005248321.1:n.430-123C>T
NM_004465.2:c.430-123C>T MANE Select	NP_004456.1:n.430-123C>T