Canonical Allele Identifier: CA116952544
Gene: IL7R HGNC NCBI

Linked Data

dbSNP Id: rs764527262
gnomAD v3: 5-35856392-C-T
gnomAD v4: 5-35856392-C-T
MyVariant Identifiers: chr5:g.35856494C>T (hg19) chr5:g.35856392C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35856392C>T , CM000667.2:g.35856392C>T GRCh38
NC_000005.9:g.35856494C>T , CM000667.1:g.35856494C>T GRCh37
NC_000005.8:g.35892251C>T NCBI36
NG_009567.1:g.4504C>T , LRG_74:g.4504C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000508941.5:c.-2+223C>T ENSP00000426426.1:n.-2+223C>T
ENST00000511031.1:n.216+3454C>T
ENST00000515665.1:c.-297C>T ENSP00000425538.1:n.-297C>T
XR_001742635.1:n.1534-2006G>A
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