Canonical Allele Identifier: CA786427785

Gene: IL21

Linked Data

• dbSNP Id: rs1157422987
• gnomAD v2: 4-123535025-G-GA
• gnomAD v3: 4-122613870-G-GA
• gnomAD v4: 4-122613870-G-GA
• MyVariant Identifiers: chr4:g.123535025_123535026insA (hg19) ; chr4:g.122613870_122613871insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613876dup , CM000666.2:g.122613876dup	GRCh38
NC_000004.11:g.123535031dup , CM000666.1:g.123535031dup	GRCh37
NC_000004.10:g.123754481dup	NCBI36
NG_031966.1:g.12187dup
NG_031966.2:g.12196dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-943dup	ENSP00000477555.1:n.361-943dup
ENST00000647784.1:n.213-943dup
ENST00000648588.1:c.361-943dup MANE Select	ENSP00000497915.1:n.361-943dup
ENST00000264497.7:c.361-943dup	ENSP00000264497.3:n.361-943dup
ENST00000611104.1:c.361-943dup	ENSP00000477555.1:n.361-943dup
NM_001207006.2:c.361-943dup	NP_001193935.1:n.361-943dup
NM_021803.3:c.361-943dup	NP_068575.1:n.361-943dup
NM_021803.4:c.361-943dup MANE Select	NP_068575.1:n.361-943dup
NM_001207006.3:c.361-943dup	NP_001193935.1:n.361-943dup