Canonical Allele Identifier: CA295269573
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs528835266
gnomAD v4: 17-82727368-C-G
MyVariant Identifiers: chr17:g.80685244C>G (hg19) chr17:g.82727368C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727368C>G , CM000679.2:g.82727368C>G GRCh38
NC_000017.10:g.80685244C>G , CM000679.1:g.80685244C>G GRCh37
NC_000017.9:g.78278533C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*197C>G MANE Select ENSP00000269373.6:n.*197C>G
ENST00000269373.10:c.*197C>G ENSP00000269373.6:n.*197C>G
ENST00000571594.1:c.53+201C>G ENSP00000459751.1:n.53+201C>G
ENST00000574832.5:c.*1084C>G ENSP00000460869.1:n.*1084C>G
NM_024619.3:c.*197C>G NP_078895.2:n.*197C>G
NR_046408.1:n.1305C>G
XM_024450948.1:c.*197C>G XP_024306716.1:n.*197C>G
NM_024619.4:c.*197C>G MANE Select NP_078895.2:n.*197C>G
NR_046408.2:n.1305C>G
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