Canonical Allele Identifier: CA364435076
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs2128261463
MyVariant Identifiers: chr6:g.52051237C>T (hg19) chr6:g.52186439C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186439C>T , CM000668.2:g.52186439C>T GRCh38
NC_000006.11:g.52051237C>T , CM000668.1:g.52051237C>T GRCh37
NC_000006.10:g.52159196C>T NCBI36
NG_033021.1:g.5053C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.8C>T MANE Select ENSP00000497968.1:p.Pro3Leu
ENST00000340057.1:c.8C>T ENSP00000344192.1:p.Pro3Leu
NM_002190.2:c.8C>T NP_002181.1:p.Pro3Leu
NM_002190.3:c.8C>T MANE Select NP_002181.1:p.Pro3Leu
Search 100 bp 5'
Search 100 bp 3'