Canonical Allele Identifier: CA3854367
Gene: IL17F HGNC NCBI

Linked Data

ClinVar Variation Id: 357469
ClinVar RCV Id: RCV000381916 RCV000456093
dbSNP Id: rs2397084
ExAC: 6:52101844 T / C
gnomAD v2: 6-52101844-T-C
gnomAD v3: 6-52237046-T-C
gnomAD v4: 6-52237046-T-C
MyVariant Identifiers: chr6:g.52101844T>C (hg19) chr6:g.52237046T>C (hg38)
PubMed: PMID:18769923
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52237046T>C , CM000668.2:g.52237046T>C GRCh38
NC_000006.11:g.52101844T>C , CM000668.1:g.52101844T>C GRCh37
NC_000006.10:g.52209803T>C NCBI36
NG_031869.1:g.12455A>G , LRG_356:g.12455A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000699946.1:c.377A>G ENSP00000514702.1:p.Glu126Gly
ENST00000336123.5:c.377A>G MANE Select ENSP00000337432.4:p.Glu126Gly
ENST00000336123.4:c.377A>G ENSP00000337432.4:p.Glu126Gly
ENST00000478427.1:n.561A>G
NM_052872.3:c.377A>G , LRG_356t1:c.377A>G NP_443104.1:p.Glu126Gly
XM_011514276.1:c.377A>G XP_011512578.1:p.Glu126Gly
NM_052872.4:c.377A>G MANE Select NP_443104.1:p.Glu126Gly
Search 100 bp 5'
Search 100 bp 3'