Canonical Allele Identifier: CA295269503
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs890808948
gnomAD v3: 17-82727203-G-T
gnomAD v4: 17-82727203-G-T
MyVariant Identifiers: chr17:g.80685079G>T (hg19) chr17:g.82727203G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727203G>T , CM000679.2:g.82727203G>T GRCh38
NC_000017.10:g.80685079G>T , CM000679.1:g.80685079G>T GRCh37
NC_000017.9:g.78278368G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*32G>T MANE Select ENSP00000269373.6:n.*32G>T
ENST00000269373.10:c.*32G>T ENSP00000269373.6:n.*32G>T
ENST00000571594.1:c.53+36G>T ENSP00000459751.1:n.53+36G>T
ENST00000574832.5:c.*919G>T ENSP00000460869.1:n.*919G>T
NM_024619.3:c.*32G>T NP_078895.2:n.*32G>T
NR_046408.1:n.1140G>T
XM_024450948.1:c.*32G>T XP_024306716.1:n.*32G>T
NM_024619.4:c.*32G>T MANE Select NP_078895.2:n.*32G>T
NR_046408.2:n.1140G>T
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