Canonical Allele Identifier: CA775764531
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1447422725
gnomAD v3: 17-82728009-G-A
gnomAD v4: 17-82728009-G-A
MyVariant Identifiers: chr17:g.80685885G>A (hg19) chr17:g.82728009G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82728009G>A , CM000679.2:g.82728009G>A GRCh38
NC_000017.10:g.80685885G>A , CM000679.1:g.80685885G>A GRCh37
NC_000017.9:g.78279174G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*838G>A MANE Select ENSP00000269373.6:n.*838G>A
ENST00000269373.10:c.*838G>A ENSP00000269373.6:n.*838G>A
ENST00000571594.1:c.53+842G>A ENSP00000459751.1:n.53+842G>A
NM_024619.3:c.*838G>A NP_078895.2:n.*838G>A
NR_046408.1:n.1946G>A
XM_024450948.1:c.*838G>A XP_024306716.1:n.*838G>A
NM_024619.4:c.*838G>A MANE Select NP_078895.2:n.*838G>A
NR_046408.2:n.1946G>A
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