Canonical Allele Identifier: CA1080102219
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752343115
gnomAD v3: 5-111071810-C-A
gnomAD v4: 5-111071810-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071810C>A , CM000667.2:g.111071810C>A GRCh38
NC_000005.9:g.110407508C>A , CM000667.1:g.110407508C>A GRCh37
NC_000005.8:g.110435407C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-81C>A MANE Select ENSP00000339804.3:n.-81C>A
ENST00000344895.3:c.-81C>A ENSP00000339804.3:n.-81C>A
ENST00000420978.6:c.35-115C>A ENSP00000399099.2:n.35-115C>A
NM_033035.4:c.-81C>A NP_149024.1:n.-81C>A
NR_045089.1:n.1439-115C>A
NM_033035.5:c.-81C>A MANE Select NP_149024.1:n.-81C>A
NR_045089.2:n.1457-115C>A
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