Canonical Allele Identifier: CA16199443
Gene: IL21 HGNC NCBI

Linked Data

dbSNP Id: rs907715

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613898C>T , CM000666.2:g.122613898C>T GRCh38
NC_000004.11:g.123535053C>T , CM000666.1:g.123535053C>T GRCh37
NC_000004.10:g.123754503C>T NCBI36
NG_031966.1:g.12160G>A
NG_031966.2:g.12169G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:n.361-970G>A ENSP00000477555.1:p.=
ENST00000647784.1:n.213-970G>A
ENST00000648588.1:c.361-970G>A MANE Select ENSP00000497915.1:p.=
ENST00000264497.7:c.361-970G>A ENSP00000264497.3:p.=
ENST00000611104.1:c.361-970G>A ENSP00000477555.1:p.=
NM_001207006.2:c.361-970G>A NP_001193935.1:p.=
NM_021803.3:c.361-970G>A NP_068575.1:p.=
NM_021803.4:c.361-970G>A MANE Select NP_068575.1:p.=
NM_001207006.3:c.361-970G>A NP_001193935.1:p.=