Canonical Allele Identifier: CA16621159
Gene: BTK HGNC NCBI

Linked Data

ClinVar Variation Id: 419415
ClinVar RCV Id: RCV000480016 RCV002250636
dbSNP Id: rs1064793859
MyVariant Identifiers: chrX:g.100614280C>T (hg19) chrX:g.101359292C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101359292C>T , CM000685.2:g.101359292C>T GRCh38
NC_000023.10:g.100614280C>T , CM000685.1:g.100614280C>T GRCh37
NC_000023.9:g.100500936C>T NCBI36
NG_009616.1:g.31933G>A , LRG_128:g.31933G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000464006.2:n.674+1G>A
ENST00000478995.2:n.1054+1G>A
ENST00000488970.2:n.1052+1G>A
ENST00000695614.1:c.894+1G>A ENSP00000512053.1:n.894+1G>A
ENST00000695615.1:c.894+1G>A ENSP00000512054.1:n.894+1G>A
ENST00000695616.1:c.*739+1G>A ENSP00000512055.1:n.*739+1G>A
ENST00000695617.1:c.891+1G>A ENSP00000512056.1:n.891+1G>A
ENST00000695618.1:c.*643+1G>A ENSP00000512058.1:n.*643+1G>A
ENST00000695619.1:c.*684+796G>A ENSP00000512059.1:n.*684+796G>A
ENST00000695620.1:c.*739+1G>A ENSP00000512060.1:n.*739+1G>A
ENST00000695621.1:c.894+1G>A ENSP00000512061.1:n.894+1G>A
ENST00000695622.1:c.831+1G>A ENSP00000512062.1:n.831+1G>A
ENST00000695623.1:c.888+1G>A ENSP00000512063.1:n.888+1G>A
ENST00000695624.1:n.199+1G>A
ENST00000695625.1:c.894+1G>A ENSP00000512064.1:n.894+1G>A
ENST00000703407.1:c.894+1G>A ENSP00000512057.1:n.894+1G>A
ENST00000308731.8:c.894+1G>A MANE Select ENSP00000308176.8:n.894+1G>A
ENST00000308731.7:c.894+1G>A ENSP00000308176.7:n.894+1G>A
ENST00000372880.5:c.894+1G>A ENSP00000361971.1:n.894+1G>A
ENST00000618050.4:c.894+1G>A ENSP00000479125.1:n.894+1G>A
ENST00000621635.4:c.996+1G>A ENSP00000483570.1:n.996+1G>A
NM_000061.2:c.894+1G>A , LRG_128t1:c.894+1G>A NP_000052.1:n.894+1G>A
NM_001287344.1:c.996+1G>A NP_001274273.1:n.996+1G>A
NM_001287345.1:c.894+1G>A NP_001274274.1:n.894+1G>A
NM_000061.3:c.894+1G>A MANE Select NP_000052.1:n.894+1G>A
NM_001287344.2:c.996+1G>A NP_001274273.1:n.996+1G>A
NM_001287345.2:c.894+1G>A NP_001274274.1:n.894+1G>A
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