Canonical Allele Identifier: CA2673772802
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs2111667923
gnomAD v4: 5-44305332-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305332T>C , CM000667.2:g.44305332T>C GRCh38
NC_000005.9:g.44305434T>C , CM000667.1:g.44305434T>C GRCh37
NC_000005.8:g.44341191T>C NCBI36
NG_011446.1:g.88351A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-140A>G MANE Select ENSP00000264664.4:n.430-140A>G
ENST00000264664.4:c.430-140A>G ENSP00000264664.4:n.430-140A>G
NM_004465.1:c.430-140A>G NP_004456.1:n.430-140A>G
XM_005248264.2:c.430-140A>G XP_005248321.1:n.430-140A>G
XM_005248264.4:c.430-140A>G XP_005248321.1:n.430-140A>G
NM_004465.2:c.430-140A>G MANE Select NP_004456.1:n.430-140A>G