Canonical Allele Identifier: CA138971026
Gene: IL17F HGNC NCBI

Linked Data

dbSNP Id: rs9382084
gnomAD v2: 6-52105667-G-T
gnomAD v3: 6-52240869-G-T
gnomAD v4: 6-52240869-G-T
MyVariant Identifiers: chr6:g.52105667G>T (hg19) chr6:g.52240869G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52240869G>T , CM000668.2:g.52240869G>T GRCh38
NC_000006.11:g.52105667G>T , CM000668.1:g.52105667G>T GRCh37
NC_000006.10:g.52213626G>T NCBI36
NG_031869.1:g.8632C>A , LRG_356:g.8632C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000699946.1:c.34-1919C>A ENSP00000514702.1:n.34-1919C>A
ENST00000336123.5:c.34-1919C>A MANE Select ENSP00000337432.4:n.34-1919C>A
ENST00000336123.4:c.34-1919C>A ENSP00000337432.4:n.34-1919C>A
NM_052872.3:c.34-1919C>A , LRG_356t1:c.34-1919C>A NP_443104.1:n.34-1919C>A
XM_011514276.1:c.34-1919C>A XP_011512578.1:n.34-1919C>A
NM_052872.4:c.34-1919C>A MANE Select NP_443104.1:n.34-1919C>A
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