Canonical Allele Identifier: CA775764284
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1208699034
gnomAD v3: 17-82727578-G-C
gnomAD v4: 17-82727578-G-C
MyVariant Identifiers: chr17:g.80685454G>C (hg19) chr17:g.82727578G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727578G>C , CM000679.2:g.82727578G>C GRCh38
NC_000017.10:g.80685454G>C , CM000679.1:g.80685454G>C GRCh37
NC_000017.9:g.78278743G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*407G>C MANE Select ENSP00000269373.6:n.*407G>C
ENST00000269373.10:c.*407G>C ENSP00000269373.6:n.*407G>C
ENST00000571594.1:c.53+411G>C ENSP00000459751.1:n.53+411G>C
NM_024619.3:c.*407G>C NP_078895.2:n.*407G>C
NR_046408.1:n.1515G>C
XM_024450948.1:c.*407G>C XP_024306716.1:n.*407G>C
NM_024619.4:c.*407G>C MANE Select NP_078895.2:n.*407G>C
NR_046408.2:n.1515G>C
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