Canonical Allele Identifier: CA558954720
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1322121170
gnomAD v2: 5-44335745-G-A
gnomAD v3: 5-44335643-G-A
gnomAD v4: 5-44335643-G-A
MyVariant Identifiers: chr5:g.44335745G>A (hg19) chr5:g.44335643G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335643G>A , CM000667.2:g.44335643G>A GRCh38
NC_000005.9:g.44335745G>A , CM000667.1:g.44335745G>A GRCh37
NC_000005.8:g.44371502G>A NCBI36
NG_011446.1:g.58040C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25113C>T MANE Select ENSP00000264664.4:n.326-25113C>T
ENST00000264664.4:c.326-25113C>T ENSP00000264664.4:n.326-25113C>T
NM_004465.1:c.326-25113C>T NP_004456.1:n.326-25113C>T
XM_005248264.2:c.326-25113C>T XP_005248321.1:n.326-25113C>T
XM_005248264.4:c.326-25113C>T XP_005248321.1:n.326-25113C>T
NM_004465.2:c.326-25113C>T MANE Select NP_004456.1:n.326-25113C>T
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