Canonical Allele Identifier: CA2674827746
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111071729-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071729C>A , CM000667.2:g.111071729C>A GRCh38
NC_000005.9:g.110407427C>A , CM000667.1:g.110407427C>A GRCh37
NC_000005.8:g.110435326C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-162C>A MANE Select ENSP00000339804.3:n.-162C>A
ENST00000344895.3:c.-162C>A ENSP00000339804.3:n.-162C>A
ENST00000420978.6:c.35-196C>A ENSP00000399099.2:n.35-196C>A
NM_033035.4:c.-162C>A NP_149024.1:n.-162C>A
NR_045089.1:n.1439-196C>A
NM_033035.5:c.-162C>A MANE Select NP_149024.1:n.-162C>A
NR_045089.2:n.1457-196C>A
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