Canonical Allele Identifier: CA1075628332

Gene: FGF10

Linked Data

• dbSNP Id: rs1740049025
• gnomAD v3: 5-44305245-A-G
• gnomAD v4: 5-44305245-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305245A>G , CM000667.2:g.44305245A>G	GRCh38
NC_000005.9:g.44305347A>G , CM000667.1:g.44305347A>G	GRCh37
NC_000005.8:g.44341104A>G	NCBI36
NG_011446.1:g.88438T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-53T>C MANE Select	ENSP00000264664.4:n.430-53T>C
ENST00000264664.4:c.430-53T>C	ENSP00000264664.4:n.430-53T>C
NM_004465.1:c.430-53T>C	NP_004456.1:n.430-53T>C
XM_005248264.2:c.430-53T>C	XP_005248321.1:n.430-53T>C
XM_005248264.4:c.430-53T>C	XP_005248321.1:n.430-53T>C
NM_004465.2:c.430-53T>C MANE Select	NP_004456.1:n.430-53T>C