Canonical Allele Identifier: CA8861086
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs762622947
ExAC: 17:80685095 C / T
gnomAD v2: 17-80685095-C-T
gnomAD v4: 17-82727219-C-T
MyVariant Identifiers: chr17:g.80685095C>T (hg19) chr17:g.82727219C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727219C>T , CM000679.2:g.82727219C>T GRCh38
NC_000017.10:g.80685095C>T , CM000679.1:g.80685095C>T GRCh37
NC_000017.9:g.78278384C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*48C>T MANE Select ENSP00000269373.6:n.*48C>T
ENST00000269373.10:c.*48C>T ENSP00000269373.6:n.*48C>T
ENST00000571594.1:c.53+52C>T ENSP00000459751.1:n.53+52C>T
ENST00000574832.5:c.*935C>T ENSP00000460869.1:n.*935C>T
NM_024619.3:c.*48C>T NP_078895.2:n.*48C>T
NR_046408.1:n.1156C>T
XM_024450948.1:c.*48C>T XP_024306716.1:n.*48C>T
NM_024619.4:c.*48C>T MANE Select NP_078895.2:n.*48C>T
NR_046408.2:n.1156C>T
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