Canonical Allele Identifier: CA1075039787
Gene: IL7R HGNC NCBI

Linked Data

dbSNP Id: rs1759635014
gnomAD v3: 5-35856390-T-C
gnomAD v4: 5-35856390-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35856390T>C , CM000667.2:g.35856390T>C GRCh38
NC_000005.9:g.35856492T>C , CM000667.1:g.35856492T>C GRCh37
NC_000005.8:g.35892249T>C NCBI36
NG_009567.1:g.4502T>C , LRG_74:g.4502T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000508941.5:c.-2+221T>C ENSP00000426426.1:n.-2+221T>C
ENST00000511031.1:n.216+3452T>C
ENST00000515665.1:c.-299T>C ENSP00000425538.1:n.-299T>C
XR_001742635.1:n.1534-2004A>G