Canonical Allele Identifier: CA359699420
Gene: FGF10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.44388564T>A (hg19) chr5:g.44388462T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388462T>A , CM000667.2:g.44388462T>A GRCh38
NC_000005.9:g.44388564T>A , CM000667.1:g.44388564T>A GRCh37
NC_000005.8:g.44424321T>A NCBI36
NG_011446.1:g.5221A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.221A>T MANE Select ENSP00000264664.4:p.Gln74Leu
ENST00000264664.4:c.221A>T ENSP00000264664.4:p.Gln74Leu
NM_004465.1:c.221A>T NP_004456.1:p.Gln74Leu
XM_005248264.2:c.221A>T XP_005248321.1:p.Gln74Leu
XM_005248264.4:c.221A>T XP_005248321.1:p.Gln74Leu
NM_004465.2:c.221A>T MANE Select NP_004456.1:p.Gln74Leu
Search 100 bp 5'
Search 100 bp 3'