Canonical Allele Identifier: CA359427024
Gene: IL7R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35860974C>G , CM000667.2:g.35860974C>G GRCh38
NC_000005.9:g.35861076C>G , CM000667.1:g.35861076C>G GRCh37
NC_000005.8:g.35896833C>G NCBI36
NG_009567.1:g.9086C>G , LRG_74:g.9086C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303115.8:c.205C>G MANE Select ENSP00000306157.3:p.Leu69Val
ENST00000303115.7:c.205C>G ENSP00000306157.3:p.Leu69Val
ENST00000506850.5:c.205C>G ENSP00000421207.1:p.Leu69Val
ENST00000511031.1:n.339C>G
ENST00000511982.1:c.205C>G ENSP00000425309.1:p.Leu69Val
ENST00000514217.5:c.205C>G ENSP00000427688.1:p.Leu69Val
NM_002185.3:c.205C>G NP_002176.2:p.Leu69Val
NR_120485.1:n.308C>G
XM_005248299.2:c.205C>G XP_005248356.1:p.Leu69Val
XM_005248300.1:c.205C>G XP_005248357.1:p.Leu69Val
XM_011514037.1:c.205C>G XP_011512339.1:p.Leu69Val
NM_002185.4:c.205C>G NP_002176.2:p.Leu69Val
NR_120485.2:n.334C>G
XM_005248299.4:c.205C>G XP_005248356.1:p.Leu69Val
NM_002185.5:c.205C>G MANE Select NP_002176.2:p.Leu69Val
NR_120485.3:n.292C>G
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