Canonical Allele Identifier: CA1628674764
Gene: IL17A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52186452A= , CM000668.2:g.52186452A= GRCh38
NC_000006.11:g.52051250A= , CM000668.1:g.52051250A= GRCh37
NC_000006.10:g.52159209A= NCBI36
NG_033021.1:g.5066A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648244.1:c.21A= MANE Select ENSP00000497968.1:p.Ser7=
ENST00000340057.1:c.21A= ENSP00000344192.1:p.Ser7=
NM_002190.2:c.21A= NP_002181.1:p.Ser7=
NM_002190.3:c.21A= MANE Select NP_002181.1:p.Ser7=