Canonical Allele Identifier: CA825771037
Gene: IL17F HGNC NCBI

Linked Data

dbSNP Id: rs9382084
gnomAD v3: 6-52240869-G-A
gnomAD v4: 6-52240869-G-A

Genomic Alleles

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

Transcript Alleles

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