Canonical Allele Identifier: CA775764489
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1471877074
gnomAD v3: 17-82727962-C-G
gnomAD v4: 17-82727962-C-G
MyVariant Identifiers: chr17:g.80685838C>G (hg19) chr17:g.82727962C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727962C>G , CM000679.2:g.82727962C>G GRCh38
NC_000017.10:g.80685838C>G , CM000679.1:g.80685838C>G GRCh37
NC_000017.9:g.78279127C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*791C>G MANE Select ENSP00000269373.6:n.*791C>G
ENST00000269373.10:c.*791C>G ENSP00000269373.6:n.*791C>G
ENST00000571594.1:c.53+795C>G ENSP00000459751.1:n.53+795C>G
NM_024619.3:c.*791C>G NP_078895.2:n.*791C>G
NR_046408.1:n.1899C>G
XM_024450948.1:c.*791C>G XP_024306716.1:n.*791C>G
NM_024619.4:c.*791C>G MANE Select NP_078895.2:n.*791C>G
NR_046408.2:n.1899C>G
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