Canonical Allele Identifier: CA443893171
Gene: IL7R HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.35877920A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35877818A>G , CM000667.2:g.35877818A>G GRCh38
NC_000005.9:g.35877920A>G , CM000667.1:g.35877920A>G GRCh37
NC_000005.8:g.35913677A>G NCBI36
NG_009567.1:g.25930A>G , LRG_74:g.25930A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.*1332A>G MANE Select ENSP00000306157.3:n.*1332A>G
ENST00000303115.7:c.*1332A>G ENSP00000306157.3:n.*1332A>G
NM_002185.3:c.*1332A>G NP_002176.2:n.*1332A>G
NR_120485.1:n.2552A>G
NM_002185.4:c.*1332A>G NP_002176.2:n.*1332A>G
NR_120485.2:n.2578A>G
XM_005248299.4:c.*1829A>G XP_005248356.1:n.*1829A>G
NM_002185.5:c.*1332A>G MANE Select NP_002176.2:n.*1332A>G
NR_120485.3:n.2536A>G
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