Canonical Allele Identifier: CA359430531
Gene: IL7R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35873479G>A , CM000667.2:g.35873479G>A GRCh38
NC_000005.9:g.35873581G>A , CM000667.1:g.35873581G>A GRCh37
NC_000005.8:g.35909338G>A NCBI36
NG_009567.1:g.21591G>A , LRG_74:g.21591G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002185.5:c.538-1G>A MANE Select NP_002176.2:n.538-1G>A
ENST00000303115.8:c.538-1G>A MANE Select ENSP00000306157.3:n.538-1G>A
NM_002185.3:c.538-1G>A NP_002176.2:n.538-1G>A
NM_002185.4:c.538-1G>A NP_002176.2:n.538-1G>A
NR_120485.1:n.641-2033G>A
NR_120485.2:n.667-2033G>A
NR_120485.3:n.625-2033G>A
ENST00000303115.7:c.538-1G>A ENSP00000306157.3:n.538-1G>A
ENST00000506850.5:c.538-1G>A ENSP00000421207.1:n.538-1G>A
ENST00000509668.1:n.279G>A
ENST00000514217.5:c.538-2033G>A ENSP00000427688.1:n.538-2033G>A
XM_005248299.2:c.538-1G>A XP_005248356.1:n.538-1G>A
XM_005248299.4:c.538-1G>A XP_005248356.1:n.538-1G>A
XM_005248300.1:c.538-1G>A XP_005248357.1:n.538-1G>A
XM_011514037.1:c.538-1G>A XP_011512339.1:n.538-1G>A
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