Canonical Allele Identifier: CA2674827785
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs2112541325
gnomAD v4: 5-111071773-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071773C>A , CM000667.2:g.111071773C>A GRCh38
NC_000005.9:g.110407471C>A , CM000667.1:g.110407471C>A GRCh37
NC_000005.8:g.110435370C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-118C>A MANE Select ENSP00000339804.3:n.-118C>A
ENST00000344895.3:c.-118C>A ENSP00000339804.3:n.-118C>A
ENST00000420978.6:c.35-152C>A ENSP00000399099.2:n.35-152C>A
NM_033035.4:c.-118C>A NP_149024.1:n.-118C>A
NR_045089.1:n.1439-152C>A
NM_033035.5:c.-118C>A MANE Select NP_149024.1:n.-118C>A
NR_045089.2:n.1457-152C>A
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