Canonical Allele Identifier: CA295269536
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs76587147
gnomAD v2: 17-80685187-A-G
gnomAD v3: 17-82727311-A-G
gnomAD v4: 17-82727311-A-G
MyVariant Identifiers: chr17:g.80685187A>G (hg19) chr17:g.82727311A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727311A>G , CM000679.2:g.82727311A>G GRCh38
NC_000017.10:g.80685187A>G , CM000679.1:g.80685187A>G GRCh37
NC_000017.9:g.78278476A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*140A>G MANE Select ENSP00000269373.6:n.*140A>G
ENST00000269373.10:c.*140A>G ENSP00000269373.6:n.*140A>G
ENST00000571594.1:c.53+144A>G ENSP00000459751.1:n.53+144A>G
ENST00000574832.5:c.*1027A>G ENSP00000460869.1:n.*1027A>G
NM_024619.3:c.*140A>G NP_078895.2:n.*140A>G
NR_046408.1:n.1248A>G
XM_024450948.1:c.*140A>G XP_024306716.1:n.*140A>G
NM_024619.4:c.*140A>G MANE Select NP_078895.2:n.*140A>G
NR_046408.2:n.1248A>G
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