Canonical Allele Identifier: CA561869647
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1483987864
gnomAD v2: 5-110408199-A-AT
gnomAD v3: 5-111072501-A-AT
gnomAD v4: 5-111072501-A-AT
MyVariant Identifiers: chr5:g.110408200_110408201insT (hg19) chr5:g.111072502_111072503insT (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-379dup MANE Select ENSP00000339804.3:n.172-379dup
ENST00000344895.3:c.172-379dup ENSP00000339804.3:n.172-379dup
ENST00000420978.6:c.172-379dup ENSP00000399099.2:n.172-379dup
NM_033035.4:c.172-379dup NP_149024.1:n.172-379dup
NR_045089.1:n.1576-379dup
NM_033035.5:c.172-379dup MANE Select NP_149024.1:n.172-379dup
NR_045089.2:n.1594-379dup
Search 100 bp 5'
Search 100 bp 3'