Canonical Allele Identifier: CA2581501993
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072481C>G , CM000667.2:g.111072481C>G GRCh38
NC_000005.9:g.110408179C>G , CM000667.1:g.110408179C>G GRCh37
NC_000005.8:g.110436078C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-407C>G MANE Select ENSP00000339804.3:n.172-407C>G
ENST00000344895.3:c.172-407C>G ENSP00000339804.3:n.172-407C>G
ENST00000420978.6:c.172-407C>G ENSP00000399099.2:n.172-407C>G
NM_033035.4:c.172-407C>G NP_149024.1:n.172-407C>G
NR_045089.1:n.1576-407C>G
NM_033035.5:c.172-407C>G MANE Select NP_149024.1:n.172-407C>G
NR_045089.2:n.1594-407C>G
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