Canonical Allele Identifier: CA1067486272

Gene: IL21

Linked Data

• dbSNP Id: rs1799298643
• gnomAD v3: 4-122613843-T-C
• gnomAD v4: 4-122613843-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613843T>C , CM000666.2:g.122613843T>C	GRCh38
NC_000004.11:g.123534998T>C , CM000666.1:g.123534998T>C	GRCh37
NC_000004.10:g.123754448T>C	NCBI36
NG_031966.1:g.12215A>G
NG_031966.2:g.12224A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-915A>G	ENSP00000477555.1:n.361-915A>G
ENST00000647784.1:n.213-915A>G
ENST00000648588.1:c.361-915A>G MANE Select	ENSP00000497915.1:n.361-915A>G
ENST00000264497.7:c.361-915A>G	ENSP00000264497.3:n.361-915A>G
ENST00000611104.1:c.361-915A>G	ENSP00000477555.1:n.361-915A>G
NM_001207006.2:c.361-915A>G	NP_001193935.1:n.361-915A>G
NM_021803.3:c.361-915A>G	NP_068575.1:n.361-915A>G
NM_021803.4:c.361-915A>G MANE Select	NP_068575.1:n.361-915A>G
NM_001207006.3:c.361-915A>G	NP_001193935.1:n.361-915A>G