Canonical Allele Identifier: CA118168754

Gene: FGF10

Linked Data

• dbSNP Id: rs10805683
• gnomAD v2: 5-44375270-C-G
• gnomAD v3: 5-44375168-C-G
• gnomAD v4: 5-44375168-C-G
• MyVariant Identifiers: chr5:g.44375270C>G (hg19) ; chr5:g.44375168C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44375168C>G , CM000667.2:g.44375168C>G	GRCh38
NC_000005.9:g.44375270C>G , CM000667.1:g.44375270C>G	GRCh37
NC_000005.8:g.44411027C>G	NCBI36
NG_011446.1:g.18515G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.325+13190G>C MANE Select	ENSP00000264664.4:n.325+13190G>C
ENST00000264664.4:c.325+13190G>C	ENSP00000264664.4:n.325+13190G>C
NM_004465.1:c.325+13190G>C	NP_004456.1:n.325+13190G>C
XM_005248264.2:c.325+13190G>C	XP_005248321.1:n.325+13190G>C
XM_005248264.4:c.325+13190G>C	XP_005248321.1:n.325+13190G>C
NM_004465.2:c.325+13190G>C MANE Select	NP_004456.1:n.325+13190G>C