Canonical Allele Identifier: CA554478152

Gene: IL21

Linked Data

• dbSNP Id: rs1439202570
• gnomAD v2: 4-123535035-G-A
• gnomAD v3: 4-122613880-G-A
• gnomAD v4: 4-122613880-G-A
• MyVariant Identifiers: chr4:g.123535035G>A (hg19) ; chr4:g.122613880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613880G>A , CM000666.2:g.122613880G>A	GRCh38
NC_000004.11:g.123535035G>A , CM000666.1:g.123535035G>A	GRCh37
NC_000004.10:g.123754485G>A	NCBI36
NG_031966.1:g.12178C>T
NG_031966.2:g.12187C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-952C>T	ENSP00000477555.1:n.361-952C>T
ENST00000647784.1:n.213-952C>T
ENST00000648588.1:c.361-952C>T MANE Select	ENSP00000497915.1:n.361-952C>T
ENST00000264497.7:c.361-952C>T	ENSP00000264497.3:n.361-952C>T
ENST00000611104.1:c.361-952C>T	ENSP00000477555.1:n.361-952C>T
NM_001207006.2:c.361-952C>T	NP_001193935.1:n.361-952C>T
NM_021803.3:c.361-952C>T	NP_068575.1:n.361-952C>T
NM_021803.4:c.361-952C>T MANE Select	NP_068575.1:n.361-952C>T
NM_001207006.3:c.361-952C>T	NP_001193935.1:n.361-952C>T