Canonical Allele Identifier: CA775764081
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1409982721
gnomAD v3: 17-82727273-G-T
gnomAD v4: 17-82727273-G-T
MyVariant Identifiers: chr17:g.80685149G>T (hg19) chr17:g.82727273G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727273G>T , CM000679.2:g.82727273G>T GRCh38
NC_000017.10:g.80685149G>T , CM000679.1:g.80685149G>T GRCh37
NC_000017.9:g.78278438G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*102G>T MANE Select ENSP00000269373.6:n.*102G>T
ENST00000269373.10:c.*102G>T ENSP00000269373.6:n.*102G>T
ENST00000571594.1:c.53+106G>T ENSP00000459751.1:n.53+106G>T
ENST00000574832.5:c.*989G>T ENSP00000460869.1:n.*989G>T
NM_024619.3:c.*102G>T NP_078895.2:n.*102G>T
NR_046408.1:n.1210G>T
XM_024450948.1:c.*102G>T XP_024306716.1:n.*102G>T
NM_024619.4:c.*102G>T MANE Select NP_078895.2:n.*102G>T
NR_046408.2:n.1210G>T
Search 100 bp 5'
Search 100 bp 3'