Canonical Allele Identifier: CA2580590347
Gene: IL7R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35877812A>C , CM000667.2:g.35877812A>C GRCh38
NC_000005.9:g.35877914A>C , CM000667.1:g.35877914A>C GRCh37
NC_000005.8:g.35913671A>C NCBI36
NG_009567.1:g.25924A>C , LRG_74:g.25924A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303115.8:c.*1326A>C MANE Select ENSP00000306157.3:n.*1326A>C
ENST00000303115.7:c.*1326A>C ENSP00000306157.3:n.*1326A>C
NM_002185.3:c.*1326A>C NP_002176.2:n.*1326A>C
NR_120485.1:n.2546A>C
NM_002185.4:c.*1326A>C NP_002176.2:n.*1326A>C
NR_120485.2:n.2572A>C
XM_005248299.4:c.*1823A>C XP_005248356.1:n.*1823A>C
NM_002185.5:c.*1326A>C MANE Select NP_002176.2:n.*1326A>C
NR_120485.3:n.2530A>C