Canonical Allele Identifier: CA118164196

Gene: FGF10

Linked Data

• dbSNP Id: rs925056187
• MyVariant Identifiers: chr5:g.44335661A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44335661A>C , CM000667.2:g.44335661A>C	GRCh38
NC_000005.9:g.44335763A>C , CM000667.1:g.44335763A>C	GRCh37
NC_000005.8:g.44371520A>C	NCBI36
NG_011446.1:g.58022T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.326-25131T>G MANE Select	ENSP00000264664.4:n.326-25131T>G
ENST00000264664.4:c.326-25131T>G	ENSP00000264664.4:n.326-25131T>G
NM_004465.1:c.326-25131T>G	NP_004456.1:n.326-25131T>G
XM_005248264.2:c.326-25131T>G	XP_005248321.1:n.326-25131T>G
XM_005248264.4:c.326-25131T>G	XP_005248321.1:n.326-25131T>G
NM_004465.2:c.326-25131T>G MANE Select	NP_004456.1:n.326-25131T>G