Canonical Allele Identifier: CA1490361170
Gene: IL21 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613708T= , CM000666.2:g.122613708T= GRCh38
NC_000004.11:g.123534863T= , CM000666.1:g.123534863T= GRCh37
NC_000004.10:g.123754313T= NCBI36
NG_031966.1:g.12350A=
NG_031966.2:g.12359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000611104.2:c.361-780A= ENSP00000477555.1:n.361-780A=
ENST00000647784.1:n.213-780A=
ENST00000648588.1:c.361-780A= MANE Select ENSP00000497915.1:n.361-780A=
ENST00000264497.7:c.361-780A= ENSP00000264497.3:n.361-780A=
ENST00000611104.1:c.361-780A= ENSP00000477555.1:n.361-780A=
NM_001207006.2:c.361-780A= NP_001193935.1:n.361-780A=
NM_021803.3:c.361-780A= NP_068575.1:n.361-780A=
NM_021803.4:c.361-780A= MANE Select NP_068575.1:n.361-780A=
NM_001207006.3:c.361-780A= NP_001193935.1:n.361-780A=
Search 100 bp 5'
Search 100 bp 3'