Canonical Allele Identifier: CA359697887
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs2111667210
gnomAD v4: 5-44305177-C-A
COSMIC: COSM3342865
MyVariant Identifiers: chr5:g.44305279C>A (hg19) chr5:g.44305177C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305177C>A , CM000667.2:g.44305177C>A GRCh38
NC_000005.9:g.44305279C>A , CM000667.1:g.44305279C>A GRCh37
NC_000005.8:g.44341036C>A NCBI36
NG_011446.1:g.88506G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.445G>T MANE Select ENSP00000264664.4:p.Asp149Tyr
ENST00000264664.4:c.445G>T ENSP00000264664.4:p.Asp149Tyr
NM_004465.1:c.445G>T NP_004456.1:p.Asp149Tyr
XM_005248264.2:c.445G>T XP_005248321.1:p.Asp149Tyr
XM_005248264.4:c.445G>T XP_005248321.1:p.Asp149Tyr
NM_004465.2:c.445G>T MANE Select NP_004456.1:p.Asp149Tyr
Search 100 bp 5'
Search 100 bp 3'