Canonical Allele Identifier: CA295269916
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1005345111
gnomAD v3: 17-82727907-T-C
gnomAD v4: 17-82727907-T-C
MyVariant Identifiers: chr17:g.80685783T>C (hg19) chr17:g.82727907T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727907T>C , CM000679.2:g.82727907T>C GRCh38
NC_000017.10:g.80685783T>C , CM000679.1:g.80685783T>C GRCh37
NC_000017.9:g.78279072T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*736T>C MANE Select ENSP00000269373.6:n.*736T>C
ENST00000269373.10:c.*736T>C ENSP00000269373.6:n.*736T>C
ENST00000571594.1:c.53+740T>C ENSP00000459751.1:n.53+740T>C
NM_024619.3:c.*736T>C NP_078895.2:n.*736T>C
NR_046408.1:n.1844T>C
XM_024450948.1:c.*736T>C XP_024306716.1:n.*736T>C
NM_024619.4:c.*736T>C MANE Select NP_078895.2:n.*736T>C
NR_046408.2:n.1844T>C
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