Canonical Allele Identifier: CA3854185
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs757834044
ExAC: 6:52051222 AAAC / A
gnomAD v2: 6-52051222-AAAC-A
gnomAD v3: 6-52186424-AAAC-A
gnomAD v4: 6-52186424-AAAC-A
MyVariant Identifiers: chr6:g.52051223_52051225del (hg19) chr6:g.52186425_52186427del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186428_52186430del , CM000668.2:g.52186428_52186430del GRCh38
NC_000006.11:g.52051226_52051228del , CM000668.1:g.52051226_52051228del GRCh37
NC_000006.10:g.52159185_52159187del NCBI36
NG_033021.1:g.5042_5044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-4_-2del MANE Select ENSP00000497968.1:n.-4_-2del
ENST00000340057.1:c.-4_-2del ENSP00000344192.1:n.-4_-2del
NM_002190.2:c.-4_-2del NP_002181.1:n.-4_-2del
NM_002190.3:c.-4_-2del MANE Select NP_002181.1:n.-4_-2del
Search 100 bp 5'
Search 100 bp 3'