Canonical Allele Identifier: CA986961928
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs2046845247
gnomAD v3: 17-82727245-C-T
gnomAD v4: 17-82727245-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727245C>T , CM000679.2:g.82727245C>T GRCh38
NC_000017.10:g.80685121C>T , CM000679.1:g.80685121C>T GRCh37
NC_000017.9:g.78278410C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*74C>T MANE Select ENSP00000269373.6:n.*74C>T
ENST00000269373.10:c.*74C>T ENSP00000269373.6:n.*74C>T
ENST00000571594.1:c.53+78C>T ENSP00000459751.1:n.53+78C>T
ENST00000574832.5:c.*961C>T ENSP00000460869.1:n.*961C>T
NM_024619.3:c.*74C>T NP_078895.2:n.*74C>T
NR_046408.1:n.1182C>T
XM_024450948.1:c.*74C>T XP_024306716.1:n.*74C>T
NM_024619.4:c.*74C>T MANE Select NP_078895.2:n.*74C>T
NR_046408.2:n.1182C>T
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