Canonical Allele Identifier: CA118164192
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs906618613
gnomAD v3: 5-44335624-G-A
gnomAD v4: 5-44335624-G-A
MyVariant Identifiers: chr5:g.44335726G>A (hg19) chr5:g.44335624G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335624G>A , CM000667.2:g.44335624G>A GRCh38
NC_000005.9:g.44335726G>A , CM000667.1:g.44335726G>A GRCh37
NC_000005.8:g.44371483G>A NCBI36
NG_011446.1:g.58059C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25094C>T MANE Select ENSP00000264664.4:n.326-25094C>T
ENST00000264664.4:c.326-25094C>T ENSP00000264664.4:n.326-25094C>T
NM_004465.1:c.326-25094C>T NP_004456.1:n.326-25094C>T
XM_005248264.2:c.326-25094C>T XP_005248321.1:n.326-25094C>T
XM_005248264.4:c.326-25094C>T XP_005248321.1:n.326-25094C>T
NM_004465.2:c.326-25094C>T MANE Select NP_004456.1:n.326-25094C>T
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