Canonical Allele Identifier: CA1075634252
Gene: FGF10 HGNC NCBI

Linked Data

gnomAD v3: 5-44365372-A-G
gnomAD v4: 5-44365372-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365372A>G , CM000667.2:g.44365372A>G GRCh38
NC_000005.9:g.44365474A>G , CM000667.1:g.44365474A>G GRCh37
NC_000005.8:g.44401231A>G NCBI36
NG_011446.1:g.28311T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+22986T>C MANE Select ENSP00000264664.4:n.325+22986T>C
ENST00000264664.4:c.325+22986T>C ENSP00000264664.4:n.325+22986T>C
NM_004465.1:c.325+22986T>C NP_004456.1:n.325+22986T>C
XM_005248264.2:c.325+22986T>C XP_005248321.1:n.325+22986T>C
XM_005248264.4:c.325+22986T>C XP_005248321.1:n.325+22986T>C
NM_004465.2:c.325+22986T>C MANE Select NP_004456.1:n.325+22986T>C
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