Canonical Allele Identifier: CA1490362831
Gene: IL21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122617757C>A , CM000666.2:g.122617757C>A GRCh38
NC_000004.11:g.123538912C>A , CM000666.1:g.123538912C>A GRCh37
NC_000004.10:g.123758362C>A NCBI36
NG_031966.1:g.8301G>T
NG_031966.2:g.8310G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000611104.2:c.205-1920G>T ENSP00000477555.1:n.205-1920G>T
ENST00000647784.1:n.56+1082G>T
ENST00000648588.1:c.205-1920G>T MANE Select ENSP00000497915.1:n.205-1920G>T
ENST00000264497.7:c.205-1920G>T ENSP00000264497.3:n.205-1920G>T
ENST00000611104.1:c.205-1920G>T ENSP00000477555.1:n.205-1920G>T
NM_001207006.2:c.205-1920G>T NP_001193935.1:n.205-1920G>T
NM_021803.3:c.205-1920G>T NP_068575.1:n.205-1920G>T
NM_021803.4:c.205-1920G>T MANE Select NP_068575.1:n.205-1920G>T
NM_001207006.3:c.205-1920G>T NP_001193935.1:n.205-1920G>T