Canonical Allele Identifier: CA561869646
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1483987864
gnomAD v2: 5-110408199-AT-A
gnomAD v3: 5-111072501-AT-A
gnomAD v4: 5-111072501-AT-A
MyVariant Identifiers: chr5:g.110408200del (hg19) chr5:g.111072502del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072509del , CM000667.2:g.111072509del GRCh38
NC_000005.9:g.110408207del , CM000667.1:g.110408207del GRCh37
NC_000005.8:g.110436106del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-379del MANE Select ENSP00000339804.3:n.172-379del
ENST00000344895.3:c.172-379del ENSP00000339804.3:n.172-379del
ENST00000420978.6:c.172-379del ENSP00000399099.2:n.172-379del
NM_033035.4:c.172-379del NP_149024.1:n.172-379del
NR_045089.1:n.1576-379del
NM_033035.5:c.172-379del MANE Select NP_149024.1:n.172-379del
NR_045089.2:n.1594-379del
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