Canonical Allele Identifier: CA138970319
Gene: IL17F HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.52239311C>T
GRCh37 chr6:g.52104109C>T
gnomAD v2:
6:52104109 C / T
gnomAD v3:
6:52239311 C / T
gnomAD v4:
chr6-52239311-C-T
Joint Max Group AF 0.00000989 (NFE)
Genomes Max Group AF 0.00000801 (AFR)
Exomes Max Group AF 0.00001177 (NFE)
dbSNP:
7771466
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52239311C>T , CM000668.2:g.52239311C>T GRCh38
NC_000006.11:g.52104109C>T , CM000668.1:g.52104109C>T GRCh37
NC_000006.10:g.52212068C>T NCBI36
NG_031869.1:g.10190G>A , LRG_356:g.10190G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699946.1:c.34-361G>A ENSP00000514702.1:n.34-361G>A
ENST00000336123.5:c.34-361G>A MANE Select ENSP00000337432.4:n.34-361G>A
ENST00000336123.4:c.34-361G>A ENSP00000337432.4:n.34-361G>A
NM_052872.3:c.34-361G>A , LRG_356t1:c.34-361G>A NP_443104.1:n.34-361G>A
XM_011514276.1:c.34-361G>A XP_011512578.1:n.34-361G>A
NM_052872.4:c.34-361G>A MANE Select NP_443104.1:n.34-361G>A
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