Canonical Allele Identifier: CA775764289
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1383555718
gnomAD v3: 17-82727608-T-G
gnomAD v4: 17-82727608-T-G
MyVariant Identifiers: chr17:g.80685484T>G (hg19) chr17:g.82727608T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727608T>G , CM000679.2:g.82727608T>G GRCh38
NC_000017.10:g.80685484T>G , CM000679.1:g.80685484T>G GRCh37
NC_000017.9:g.78278773T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*437T>G MANE Select ENSP00000269373.6:n.*437T>G
ENST00000269373.10:c.*437T>G ENSP00000269373.6:n.*437T>G
ENST00000571594.1:c.53+441T>G ENSP00000459751.1:n.53+441T>G
NM_024619.3:c.*437T>G NP_078895.2:n.*437T>G
NR_046408.1:n.1545T>G
XM_024450948.1:c.*437T>G XP_024306716.1:n.*437T>G
NM_024619.4:c.*437T>G MANE Select NP_078895.2:n.*437T>G
NR_046408.2:n.1545T>G
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