Canonical Allele Identifier: CA986962233
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs2046850257
gnomAD v3: 17-82727911-C-T
gnomAD v4: 17-82727911-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727911C>T , CM000679.2:g.82727911C>T GRCh38
NC_000017.10:g.80685787C>T , CM000679.1:g.80685787C>T GRCh37
NC_000017.9:g.78279076C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*740C>T MANE Select ENSP00000269373.6:n.*740C>T
ENST00000269373.10:c.*740C>T ENSP00000269373.6:n.*740C>T
ENST00000571594.1:c.53+744C>T ENSP00000459751.1:n.53+744C>T
NM_024619.3:c.*740C>T NP_078895.2:n.*740C>T
NR_046408.1:n.1848C>T
XM_024450948.1:c.*740C>T XP_024306716.1:n.*740C>T
NM_024619.4:c.*740C>T MANE Select NP_078895.2:n.*740C>T
NR_046408.2:n.1848C>T
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