Canonical Allele Identifier: CA1628674550
Gene: IL17A HGNC NCBI

Linked Data

dbSNP Id: rs947815261
gnomAD v4: 6-52186375-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186375G>T , CM000668.2:g.52186375G>T GRCh38
NC_000006.11:g.52051173G>T , CM000668.1:g.52051173G>T GRCh37
NC_000006.10:g.52159132G>T NCBI36
NG_033021.1:g.4989G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.-57G>T MANE Select ENSP00000497968.1:n.-57G>T
NM_002190.3:c.-57G>T MANE Select NP_002181.1:n.-57G>T