Canonical Allele Identifier: CA2707165838

Gene: IL21

Linked Data

• dbSNP Id: rs2150685358

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613713A>G , CM000666.2:g.122613713A>G	GRCh38
NC_000004.11:g.123534868A>G , CM000666.1:g.123534868A>G	GRCh37
NC_000004.10:g.123754318A>G	NCBI36
NG_031966.1:g.12345T>C
NG_031966.2:g.12354T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000611104.2:c.361-785T>C	ENSP00000477555.1:n.361-785T>C
ENST00000647784.1:n.213-785T>C
ENST00000648588.1:c.361-785T>C MANE Select	ENSP00000497915.1:n.361-785T>C
ENST00000264497.7:c.361-785T>C	ENSP00000264497.3:n.361-785T>C
ENST00000611104.1:c.361-785T>C	ENSP00000477555.1:n.361-785T>C
NM_001207006.2:c.361-785T>C	NP_001193935.1:n.361-785T>C
NM_021803.3:c.361-785T>C	NP_068575.1:n.361-785T>C
NM_021803.4:c.361-785T>C MANE Select	NP_068575.1:n.361-785T>C
NM_001207006.3:c.361-785T>C	NP_001193935.1:n.361-785T>C