Canonical Allele Identifier: CA118166979
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs924356910
gnomAD v3: 5-44359377-A-G
gnomAD v4: 5-44359377-A-G
MyVariant Identifiers: chr5:g.44359479A>G (hg19) chr5:g.44359377A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359377A>G , CM000667.2:g.44359377A>G GRCh38
NC_000005.9:g.44359479A>G , CM000667.1:g.44359479A>G GRCh37
NC_000005.8:g.44395236A>G NCBI36
NG_011446.1:g.34306T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+28981T>C MANE Select ENSP00000264664.4:n.325+28981T>C
ENST00000264664.4:c.325+28981T>C ENSP00000264664.4:n.325+28981T>C
NM_004465.1:c.325+28981T>C NP_004456.1:n.325+28981T>C
XM_005248264.2:c.325+28981T>C XP_005248321.1:n.325+28981T>C
XM_005248264.4:c.325+28981T>C XP_005248321.1:n.325+28981T>C
NM_004465.2:c.325+28981T>C MANE Select NP_004456.1:n.325+28981T>C
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