Canonical Allele Identifier: CA2674829138
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111077855-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077855C>T , CM000667.2:g.111077855C>T GRCh38
NC_000005.9:g.110413553C>T , CM000667.1:g.110413553C>T GRCh37
NC_000005.8:g.110441452C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1781C>T MANE Select ENSP00000339804.3:n.*1781C>T
ENST00000379706.4:c.*1781C>T ENSP00000427827.1:n.*1781C>T
NM_033035.4:c.*1781C>T NP_149024.1:n.*1781C>T
NM_138551.4:c.*1781C>T NP_612561.2:n.*1781C>T
NR_045089.1:n.3665C>T
NM_033035.5:c.*1781C>T MANE Select NP_149024.1:n.*1781C>T
NM_138551.5:c.*1781C>T NP_612561.2:n.*1781C>T
NR_045089.2:n.3683C>T
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