Canonical Allele Identifier: CA1490361219
Gene: IL21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613805G= , CM000666.2:g.122613805G= GRCh38
NC_000004.11:g.123534960G= , CM000666.1:g.123534960G= GRCh37
NC_000004.10:g.123754410G= NCBI36
NG_031966.1:g.12253C=
NG_031966.2:g.12262C=

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-877C= ENSP00000477555.1:n.361-877C=
ENST00000647784.1:n.213-877C=
ENST00000648588.1:c.361-877C= MANE Select ENSP00000497915.1:n.361-877C=
ENST00000264497.7:c.361-877C= ENSP00000264497.3:n.361-877C=
ENST00000611104.1:c.361-877C= ENSP00000477555.1:n.361-877C=
NM_001207006.2:c.361-877C= NP_001193935.1:n.361-877C=
NM_021803.3:c.361-877C= NP_068575.1:n.361-877C=
NM_021803.4:c.361-877C= MANE Select NP_068575.1:n.361-877C=
NM_001207006.3:c.361-877C= NP_001193935.1:n.361-877C=