Canonical Allele Identifier: CA1543136989
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1561218921
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44375109T>C , CM000667.2:g.44375109T>C GRCh38
NC_000005.9:g.44375211T>C , CM000667.1:g.44375211T>C GRCh37
NC_000005.8:g.44410968T>C NCBI36
NG_011446.1:g.18574A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+13249A>G MANE Select ENSP00000264664.4:n.325+13249A>G
ENST00000264664.4:c.325+13249A>G ENSP00000264664.4:n.325+13249A>G
NM_004465.1:c.325+13249A>G NP_004456.1:n.325+13249A>G
XM_005248264.2:c.325+13249A>G XP_005248321.1:n.325+13249A>G
XM_005248264.4:c.325+13249A>G XP_005248321.1:n.325+13249A>G
NM_004465.2:c.325+13249A>G MANE Select NP_004456.1:n.325+13249A>G
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