Canonical Allele Identifier: CA10654296
Gene: IL1RAPL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 368186
ClinVar RCV Id: RCV000269165
dbSNP Id: rs143054072
gnomAD v2: X-28606150-G-A
gnomAD v3: X-28588033-G-A
gnomAD v4: X-28588033-G-A
MyVariant Identifiers: chrX:g.28606150G>A (hg19) chrX:g.28588033G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.28588033G>A , CM000685.2:g.28588033G>A GRCh38
NC_000023.10:g.28606150G>A , CM000685.1:g.28606150G>A GRCh37
NC_000023.9:g.28516071G>A NCBI36
NG_008292.1:g.5470G>A
NG_008292.2:g.5470G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.-39G>A MANE Select ENSP00000368278.1:n.-39G>A
ENST00000378993.5:c.-39G>A ENSP00000368278.1:n.-39G>A
NM_014271.3:c.-39G>A NP_055086.1:n.-39G>A
NM_014271.4:c.-39G>A MANE Select NP_055086.1:n.-39G>A
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