Canonical Allele Identifier: CA2674827798
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111071789-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071789C>G , CM000667.2:g.111071789C>G GRCh38
NC_000005.9:g.110407487C>G , CM000667.1:g.110407487C>G GRCh37
NC_000005.8:g.110435386C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-102C>G MANE Select ENSP00000339804.3:n.-102C>G
ENST00000344895.3:c.-102C>G ENSP00000339804.3:n.-102C>G
ENST00000420978.6:c.35-136C>G ENSP00000399099.2:n.35-136C>G
NM_033035.4:c.-102C>G NP_149024.1:n.-102C>G
NR_045089.1:n.1439-136C>G
NM_033035.5:c.-102C>G MANE Select NP_149024.1:n.-102C>G
NR_045089.2:n.1457-136C>G
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