Canonical Allele Identifier: CA12236544
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs10484879
gnomAD v2: 6-52051957-G-T
gnomAD v3: 6-52187159-G-T
gnomAD v4: 6-52187159-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52187159G>T , CM000668.2:g.52187159G>T GRCh38
NC_000006.11:g.52051957G>T , CM000668.1:g.52051957G>T GRCh37
NC_000006.10:g.52159916G>T NCBI36
NG_033021.1:g.5773G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648244.1:c.28-444G>T MANE Select ENSP00000497968.1:n.28-444G>T
ENST00000340057.1:c.28-444G>T ENSP00000344192.1:n.28-444G>T
NM_002190.2:c.28-444G>T NP_002181.1:n.28-444G>T
NM_002190.3:c.28-444G>T MANE Select NP_002181.1:n.28-444G>T