Canonical Allele Identifier: CA118164210
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs557059042
gnomAD v3: 5-44335814-A-C
gnomAD v4: 5-44335814-A-C
MyVariant Identifiers: chr5:g.44335916A>C (hg19) chr5:g.44335814A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335814A>C , CM000667.2:g.44335814A>C GRCh38
NC_000005.9:g.44335916A>C , CM000667.1:g.44335916A>C GRCh37
NC_000005.8:g.44371673A>C NCBI36
NG_011446.1:g.57869T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25284T>G MANE Select ENSP00000264664.4:n.326-25284T>G
ENST00000264664.4:c.326-25284T>G ENSP00000264664.4:n.326-25284T>G
NM_004465.1:c.326-25284T>G NP_004456.1:n.326-25284T>G
XM_005248264.2:c.326-25284T>G XP_005248321.1:n.326-25284T>G
XM_005248264.4:c.326-25284T>G XP_005248321.1:n.326-25284T>G
NM_004465.2:c.326-25284T>G MANE Select NP_004456.1:n.326-25284T>G
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