Canonical Allele Identifier: CA1075628408
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1056922244
gnomAD v3: 5-44305731-G-C
gnomAD v4: 5-44305731-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305731G>C , CM000667.2:g.44305731G>C GRCh38
NC_000005.9:g.44305833G>C , CM000667.1:g.44305833G>C GRCh37
NC_000005.8:g.44341590G>C NCBI36
NG_011446.1:g.87952C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-539C>G MANE Select ENSP00000264664.4:n.430-539C>G
ENST00000264664.4:c.430-539C>G ENSP00000264664.4:n.430-539C>G
NM_004465.1:c.430-539C>G NP_004456.1:n.430-539C>G
XM_005248264.2:c.430-539C>G XP_005248321.1:n.430-539C>G
XM_005248264.4:c.430-539C>G XP_005248321.1:n.430-539C>G
NM_004465.2:c.430-539C>G MANE Select NP_004456.1:n.430-539C>G
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