Canonical Allele Identifier: CA118164190
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs948205018
gnomAD v2: 5-44335722-T-A
gnomAD v3: 5-44335620-T-A
gnomAD v4: 5-44335620-T-A
MyVariant Identifiers: chr5:g.44335722T>A (hg19) chr5:g.44335620T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335620T>A , CM000667.2:g.44335620T>A GRCh38
NC_000005.9:g.44335722T>A , CM000667.1:g.44335722T>A GRCh37
NC_000005.8:g.44371479T>A NCBI36
NG_011446.1:g.58063A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25090A>T MANE Select ENSP00000264664.4:n.326-25090A>T
ENST00000264664.4:c.326-25090A>T ENSP00000264664.4:n.326-25090A>T
NM_004465.1:c.326-25090A>T NP_004456.1:n.326-25090A>T
XM_005248264.2:c.326-25090A>T XP_005248321.1:n.326-25090A>T
XM_005248264.4:c.326-25090A>T XP_005248321.1:n.326-25090A>T
NM_004465.2:c.326-25090A>T MANE Select NP_004456.1:n.326-25090A>T
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