Canonical Allele Identifier: CA295269911
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs539712281
gnomAD v2: 17-80685733-T-G
gnomAD v3: 17-82727857-T-G
gnomAD v4: 17-82727857-T-G
MyVariant Identifiers: chr17:g.80685733T>G (hg19) chr17:g.82727857T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727857T>G , CM000679.2:g.82727857T>G GRCh38
NC_000017.10:g.80685733T>G , CM000679.1:g.80685733T>G GRCh37
NC_000017.9:g.78279022T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*686T>G MANE Select ENSP00000269373.6:n.*686T>G
ENST00000269373.10:c.*686T>G ENSP00000269373.6:n.*686T>G
ENST00000571594.1:c.53+690T>G ENSP00000459751.1:n.53+690T>G
NM_024619.3:c.*686T>G NP_078895.2:n.*686T>G
NR_046408.1:n.1794T>G
XM_024450948.1:c.*686T>G XP_024306716.1:n.*686T>G
NM_024619.4:c.*686T>G MANE Select NP_078895.2:n.*686T>G
NR_046408.2:n.1794T>G
Search 100 bp 5'
Search 100 bp 3'