Canonical Allele Identifier: CA105235720

Gene: IL21

Linked Data

• dbSNP Id: rs908911118
• gnomAD v3: 4-122613823-T-C
• gnomAD v4: 4-122613823-T-C
• MyVariant Identifiers: chr4:g.123534978T>C (hg19) ; chr4:g.122613823T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613823T>C , CM000666.2:g.122613823T>C	GRCh38
NC_000004.11:g.123534978T>C , CM000666.1:g.123534978T>C	GRCh37
NC_000004.10:g.123754428T>C	NCBI36
NG_031966.1:g.12235A>G
NG_031966.2:g.12244A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-895A>G	ENSP00000477555.1:n.361-895A>G
ENST00000647784.1:n.213-895A>G
ENST00000648588.1:c.361-895A>G MANE Select	ENSP00000497915.1:n.361-895A>G
ENST00000264497.7:c.361-895A>G	ENSP00000264497.3:n.361-895A>G
ENST00000611104.1:c.361-895A>G	ENSP00000477555.1:n.361-895A>G
NM_001207006.2:c.361-895A>G	NP_001193935.1:n.361-895A>G
NM_021803.3:c.361-895A>G	NP_068575.1:n.361-895A>G
NM_021803.4:c.361-895A>G MANE Select	NP_068575.1:n.361-895A>G
NM_001207006.3:c.361-895A>G	NP_001193935.1:n.361-895A>G