Canonical Allele Identifier: CA1543090394

Gene: FGF10

Linked Data

• dbSNP Id: rs774516773
• gnomAD v4: 5-44388294-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44388294T>C , CM000667.2:g.44388294T>C	GRCh38
NC_000005.9:g.44388396T>C , CM000667.1:g.44388396T>C	GRCh37
NC_000005.8:g.44424153T>C	NCBI36
NG_011446.1:g.5389A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+64A>G MANE Select	ENSP00000264664.4:n.325+64A>G
ENST00000264664.4:c.325+64A>G	ENSP00000264664.4:n.325+64A>G
NM_004465.1:c.325+64A>G	NP_004456.1:n.325+64A>G
XM_005248264.2:c.325+64A>G	XP_005248321.1:n.325+64A>G
XM_005248264.4:c.325+64A>G	XP_005248321.1:n.325+64A>G
NM_004465.2:c.325+64A>G MANE Select	NP_004456.1:n.325+64A>G