Canonical Allele Identifier: CA118160605

Gene: FGF10

Linked Data

• dbSNP Id: rs912897536
• gnomAD v2: 5-44305757-T-A
• gnomAD v3: 5-44305655-T-A
• gnomAD v4: 5-44305655-T-A
• MyVariant Identifiers: chr5:g.44305757T>A (hg19) ; chr5:g.44305655T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305655T>A , CM000667.2:g.44305655T>A	GRCh38
NC_000005.9:g.44305757T>A , CM000667.1:g.44305757T>A	GRCh37
NC_000005.8:g.44341514T>A	NCBI36
NG_011446.1:g.88028A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.430-463A>T MANE Select	ENSP00000264664.4:n.430-463A>T
ENST00000264664.4:c.430-463A>T	ENSP00000264664.4:n.430-463A>T
NM_004465.1:c.430-463A>T	NP_004456.1:n.430-463A>T
XM_005248264.2:c.430-463A>T	XP_005248321.1:n.430-463A>T
XM_005248264.4:c.430-463A>T	XP_005248321.1:n.430-463A>T
NM_004465.2:c.430-463A>T MANE Select	NP_004456.1:n.430-463A>T