Canonical Allele Identifier: CA105235718

Gene: IL21

Linked Data

• dbSNP Id: rs570459756
• gnomAD v2: 4-123534966-A-G
• gnomAD v3: 4-122613811-A-G
• gnomAD v4: 4-122613811-A-G
• MyVariant Identifiers: chr4:g.123534966A>G (hg19) ; chr4:g.122613811A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613811A>G , CM000666.2:g.122613811A>G	GRCh38
NC_000004.11:g.123534966A>G , CM000666.1:g.123534966A>G	GRCh37
NC_000004.10:g.123754416A>G	NCBI36
NG_031966.1:g.12247T>C
NG_031966.2:g.12256T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-883T>C	ENSP00000477555.1:n.361-883T>C
ENST00000647784.1:n.213-883T>C
ENST00000648588.1:c.361-883T>C MANE Select	ENSP00000497915.1:n.361-883T>C
ENST00000264497.7:c.361-883T>C	ENSP00000264497.3:n.361-883T>C
ENST00000611104.1:c.361-883T>C	ENSP00000477555.1:n.361-883T>C
NM_001207006.2:c.361-883T>C	NP_001193935.1:n.361-883T>C
NM_021803.3:c.361-883T>C	NP_068575.1:n.361-883T>C
NM_021803.4:c.361-883T>C MANE Select	NP_068575.1:n.361-883T>C
NM_001207006.3:c.361-883T>C	NP_001193935.1:n.361-883T>C