Canonical Allele Identifier: CA3258489
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs748739422
ExAC: 5:44305271 C / T
gnomAD v2: 5-44305271-C-T
gnomAD v4: 5-44305169-C-T
MyVariant Identifiers: chr5:g.44305271C>T (hg19) chr5:g.44305169C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305169C>T , CM000667.2:g.44305169C>T GRCh38
NC_000005.9:g.44305271C>T , CM000667.1:g.44305271C>T GRCh37
NC_000005.8:g.44341028C>T NCBI36
NG_011446.1:g.88514G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.453G>A MANE Select ENSP00000264664.4:p.Lys151=
ENST00000264664.4:c.453G>A ENSP00000264664.4:p.Lys151=
NM_004465.1:c.453G>A NP_004456.1:p.Lys151=
XM_005248264.2:c.453G>A XP_005248321.1:p.Lys151=
XM_005248264.4:c.453G>A XP_005248321.1:p.Lys151=
NM_004465.2:c.453G>A MANE Select NP_004456.1:p.Lys151=
Search 100 bp 5'
Search 100 bp 3'