Canonical Allele Identifier: CA364435097
Gene: IL17A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186442G>T , CM000668.2:g.52186442G>T GRCh38
NC_000006.11:g.52051240G>T , CM000668.1:g.52051240G>T GRCh37
NC_000006.10:g.52159199G>T NCBI36
NG_033021.1:g.5056G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.11G>T MANE Select ENSP00000497968.1:p.Gly4Val
ENST00000340057.1:c.11G>T ENSP00000344192.1:p.Gly4Val
NM_002190.2:c.11G>T NP_002181.1:p.Gly4Val
NM_002190.3:c.11G>T MANE Select NP_002181.1:p.Gly4Val