Canonical Allele Identifier: CA118160606

Gene: FGF10

Linked Data

• dbSNP Id: rs947088301
• gnomAD v2: 5-44305761-T-C
• MyVariant Identifiers: chr5:g.44305761T>C (hg19) ; chr5:g.44305659T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305659T>C , CM000667.2:g.44305659T>C	GRCh38
NC_000005.9:g.44305761T>C , CM000667.1:g.44305761T>C	GRCh37
NC_000005.8:g.44341518T>C	NCBI36
NG_011446.1:g.88024A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.430-467A>G MANE Select	ENSP00000264664.4:n.430-467A>G
ENST00000264664.4:c.430-467A>G	ENSP00000264664.4:n.430-467A>G
NM_004465.1:c.430-467A>G	NP_004456.1:n.430-467A>G
XM_005248264.2:c.430-467A>G	XP_005248321.1:n.430-467A>G
XM_005248264.4:c.430-467A>G	XP_005248321.1:n.430-467A>G
NM_004465.2:c.430-467A>G MANE Select	NP_004456.1:n.430-467A>G