Canonical Allele Identifier: CA118170235
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs922473926
gnomAD v3: 5-44388293-T-A
gnomAD v4: 5-44388293-T-A
MyVariant Identifiers: chr5:g.44388395T>A (hg19) chr5:g.44388293T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388293T>A , CM000667.2:g.44388293T>A GRCh38
NC_000005.9:g.44388395T>A , CM000667.1:g.44388395T>A GRCh37
NC_000005.8:g.44424152T>A NCBI36
NG_011446.1:g.5390A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+65A>T MANE Select ENSP00000264664.4:n.325+65A>T
ENST00000264664.4:c.325+65A>T ENSP00000264664.4:n.325+65A>T
NM_004465.1:c.325+65A>T NP_004456.1:n.325+65A>T
XM_005248264.2:c.325+65A>T XP_005248321.1:n.325+65A>T
XM_005248264.4:c.325+65A>T XP_005248321.1:n.325+65A>T
NM_004465.2:c.325+65A>T MANE Select NP_004456.1:n.325+65A>T
Search 100 bp 5'
Search 100 bp 3'