Canonical Allele Identifier: CA2640698431
Gene: FN3KRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82728015G>T , CM000679.2:g.82728015G>T GRCh38
NC_000017.10:g.80685891G>T , CM000679.1:g.80685891G>T GRCh37
NC_000017.9:g.78279180G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.10:c.*844G>T ENSP00000269373.6:n.*844G>T
ENST00000571594.1:c.53+848G>T ENSP00000459751.1:n.53+848G>T
NM_024619.3:c.*844G>T NP_078895.2:n.*844G>T
NR_046408.1:n.1952G>T
XM_024450948.1:c.*844G>T XP_024306716.1:n.*844G>T