Canonical Allele Identifier: CA2673545955
Gene: IL7R HGNC NCBI

Linked Data

gnomAD v4: 5-35877843-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35877843C>A , CM000667.2:g.35877843C>A GRCh38
NC_000005.9:g.35877945C>A , CM000667.1:g.35877945C>A GRCh37
NC_000005.8:g.35913702C>A NCBI36
NG_009567.1:g.25955C>A , LRG_74:g.25955C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.*1357C>A MANE Select ENSP00000306157.3:n.*1357C>A
ENST00000303115.7:c.*1357C>A ENSP00000306157.3:n.*1357C>A
NM_002185.3:c.*1357C>A NP_002176.2:n.*1357C>A
NR_120485.1:n.2577C>A
NM_002185.4:c.*1357C>A NP_002176.2:n.*1357C>A
NR_120485.2:n.2603C>A
XM_005248299.4:c.*1854C>A XP_005248356.1:n.*1854C>A
NM_002185.5:c.*1357C>A MANE Select NP_002176.2:n.*1357C>A
NR_120485.3:n.2561C>A
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