Canonical Allele Identifier: CA1080103086
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752560517
gnomAD v3: 5-111078000-C-A
gnomAD v4: 5-111078000-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111078000C>A , CM000667.2:g.111078000C>A GRCh38
NC_000005.9:g.110413698C>A , CM000667.1:g.110413698C>A GRCh37
NC_000005.8:g.110441597C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1926C>A MANE Select ENSP00000339804.3:n.*1926C>A
ENST00000379706.4:c.*1926C>A ENSP00000427827.1:n.*1926C>A
NM_033035.4:c.*1926C>A NP_149024.1:n.*1926C>A
NM_138551.4:c.*1926C>A NP_612561.2:n.*1926C>A
NR_045089.1:n.3810C>A
NM_033035.5:c.*1926C>A MANE Select NP_149024.1:n.*1926C>A
NM_138551.5:c.*1926C>A NP_612561.2:n.*1926C>A
NR_045089.2:n.3828C>A
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