Canonical Allele Identifier: CA12436702
Gene: IL17A HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.52190537C>T
GRCh37 chr6:g.52055335C>T
gnomAD v2:
6:52055335 C / T
gnomAD v3:
6:52190537 C / T
gnomAD v4:
chr6-52190537-C-T
Joint Max Group AF 0.19242639 (SAS)
Genomes Max Group AF 0.19242639 (SAS)
Exomes Max Group AF 0.04441926 (NFE)
dbSNP:
1974226
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52190537C>T , CM000668.2:g.52190537C>T GRCh38
NC_000006.11:g.52055335C>T , CM000668.1:g.52055335C>T GRCh37
NC_000006.10:g.52163294C>T NCBI36
NG_033021.1:g.9151C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.*1245C>T MANE Select ENSP00000497968.1:n.*1245C>T
ENST00000340057.1:c.*1245C>T ENSP00000344192.1:n.*1245C>T
NM_002190.2:c.*1245C>T NP_002181.1:n.*1245C>T
NM_002190.3:c.*1245C>T MANE Select NP_002181.1:n.*1245C>T
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