Canonical Allele Identifier: CA1572616493
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752342136
gnomAD v4: 5-111071743-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071743A>T , CM000667.2:g.111071743A>T GRCh38
NC_000005.9:g.110407441A>T , CM000667.1:g.110407441A>T GRCh37
NC_000005.8:g.110435340A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-148A>T MANE Select ENSP00000339804.3:n.-148A>T
ENST00000344895.3:c.-148A>T ENSP00000339804.3:n.-148A>T
ENST00000420978.6:c.35-182A>T ENSP00000399099.2:n.35-182A>T
NM_033035.4:c.-148A>T NP_149024.1:n.-148A>T
NR_045089.1:n.1439-182A>T
NM_033035.5:c.-148A>T MANE Select NP_149024.1:n.-148A>T
NR_045089.2:n.1457-182A>T
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