Canonical Allele Identifier: CA295269506
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs981340698
gnomAD v4: 17-82727221-T-A
MyVariant Identifiers: chr17:g.80685097T>A (hg19) chr17:g.82727221T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727221T>A , CM000679.2:g.82727221T>A GRCh38
NC_000017.10:g.80685097T>A , CM000679.1:g.80685097T>A GRCh37
NC_000017.9:g.78278386T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*50T>A MANE Select ENSP00000269373.6:n.*50T>A
ENST00000269373.10:c.*50T>A ENSP00000269373.6:n.*50T>A
ENST00000571594.1:c.53+54T>A ENSP00000459751.1:n.53+54T>A
ENST00000574832.5:c.*937T>A ENSP00000460869.1:n.*937T>A
NM_024619.3:c.*50T>A NP_078895.2:n.*50T>A
NR_046408.1:n.1158T>A
XM_024450948.1:c.*50T>A XP_024306716.1:n.*50T>A
NM_024619.4:c.*50T>A MANE Select NP_078895.2:n.*50T>A
NR_046408.2:n.1158T>A
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