Canonical Allele Identifier: CA2580589723
Gene: IL21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613898C>A , CM000666.2:g.122613898C>A GRCh38
NC_000004.11:g.123535053C>A , CM000666.1:g.123535053C>A GRCh37
NC_000004.10:g.123754503C>A NCBI36
NG_031966.1:g.12160G>T
NG_031966.2:g.12169G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-970G>T ENSP00000477555.1:n.361-970G>T
ENST00000647784.1:n.213-970G>T
ENST00000648588.1:c.361-970G>T MANE Select ENSP00000497915.1:n.361-970G>T
ENST00000264497.7:c.361-970G>T ENSP00000264497.3:n.361-970G>T
ENST00000611104.1:c.361-970G>T ENSP00000477555.1:n.361-970G>T
NM_001207006.2:c.361-970G>T NP_001193935.1:n.361-970G>T
NM_021803.3:c.361-970G>T NP_068575.1:n.361-970G>T
NM_021803.4:c.361-970G>T MANE Select NP_068575.1:n.361-970G>T
NM_001207006.3:c.361-970G>T NP_001193935.1:n.361-970G>T