Canonical Allele Identifier: CA138932625
Gene: IL17A HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.52189451G>A
GRCh37 chr6:g.52054249G>A
gnomAD v2:
6:52054249 G / A
gnomAD v3:
6:52189451 G / A
gnomAD v4:
chr6-52189451-G-A
Joint Max Group AF 0.23379061 (MID)
Genomes Max Group AF 0.23402804 (NFE)
Exomes Max Group AF 0.23227684 (NFE)
ClinVar RCV:
RCV001670616
ClinVar Variation:
1266947
dbSNP:
7747909
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52189451G>A , CM000668.2:g.52189451G>A GRCh38
NC_000006.11:g.52054249G>A , CM000668.1:g.52054249G>A GRCh37
NC_000006.10:g.52162208G>A NCBI36
NG_033021.1:g.8065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.*159G>A MANE Select ENSP00000497968.1:n.*159G>A
ENST00000340057.1:c.*159G>A ENSP00000344192.1:n.*159G>A
NM_002190.2:c.*159G>A NP_002181.1:n.*159G>A
NM_002190.3:c.*159G>A MANE Select NP_002181.1:n.*159G>A
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