Canonical Allele Identifier: CA2673545951
Gene: IL7R HGNC NCBI

Linked Data

gnomAD v4: 5-35877842-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35877842G>T , CM000667.2:g.35877842G>T GRCh38
NC_000005.9:g.35877944G>T , CM000667.1:g.35877944G>T GRCh37
NC_000005.8:g.35913701G>T NCBI36
NG_009567.1:g.25954G>T , LRG_74:g.25954G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.*1356G>T MANE Select ENSP00000306157.3:n.*1356G>T
ENST00000303115.7:c.*1356G>T ENSP00000306157.3:n.*1356G>T
NM_002185.3:c.*1356G>T NP_002176.2:n.*1356G>T
NR_120485.1:n.2576G>T
NM_002185.4:c.*1356G>T NP_002176.2:n.*1356G>T
NR_120485.2:n.2602G>T
XM_005248299.4:c.*1853G>T XP_005248356.1:n.*1853G>T
NM_002185.5:c.*1356G>T MANE Select NP_002176.2:n.*1356G>T
NR_120485.3:n.2560G>T
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