Canonical Allele Identifier: CA2673545929
Gene: IL7R HGNC NCBI

Linked Data

gnomAD v4: 5-35877824-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35877824G>T , CM000667.2:g.35877824G>T GRCh38
NC_000005.9:g.35877926G>T , CM000667.1:g.35877926G>T GRCh37
NC_000005.8:g.35913683G>T NCBI36
NG_009567.1:g.25936G>T , LRG_74:g.25936G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.*1338G>T MANE Select ENSP00000306157.3:n.*1338G>T
ENST00000303115.7:c.*1338G>T ENSP00000306157.3:n.*1338G>T
NM_002185.3:c.*1338G>T NP_002176.2:n.*1338G>T
NR_120485.1:n.2558G>T
NM_002185.4:c.*1338G>T NP_002176.2:n.*1338G>T
NR_120485.2:n.2584G>T
XM_005248299.4:c.*1835G>T XP_005248356.1:n.*1835G>T
NM_002185.5:c.*1338G>T MANE Select NP_002176.2:n.*1338G>T
NR_120485.3:n.2542G>T
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