Canonical Allele Identifier: CA559293707
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1273035112
gnomAD v2: 5-44305338-C-G
gnomAD v4: 5-44305236-C-G
MyVariant Identifiers: chr5:g.44305338C>G (hg19) chr5:g.44305236C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305236C>G , CM000667.2:g.44305236C>G GRCh38
NC_000005.9:g.44305338C>G , CM000667.1:g.44305338C>G GRCh37
NC_000005.8:g.44341095C>G NCBI36
NG_011446.1:g.88447G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-44G>C MANE Select ENSP00000264664.4:n.430-44G>C
ENST00000264664.4:c.430-44G>C ENSP00000264664.4:n.430-44G>C
NM_004465.1:c.430-44G>C NP_004456.1:n.430-44G>C
XM_005248264.2:c.430-44G>C XP_005248321.1:n.430-44G>C
XM_005248264.4:c.430-44G>C XP_005248321.1:n.430-44G>C
NM_004465.2:c.430-44G>C MANE Select NP_004456.1:n.430-44G>C
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