Canonical Allele Identifier: CA124873174
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs765036707
gnomAD v4: 5-111071736-C-A
MyVariant Identifiers: chr5:g.111071736C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071736C>A , CM000667.2:g.111071736C>A GRCh38
NC_000005.9:g.110407434C>A , CM000667.1:g.110407434C>A GRCh37
NC_000005.8:g.110435333C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-155C>A MANE Select ENSP00000339804.3:n.-155C>A
ENST00000344895.3:c.-155C>A ENSP00000339804.3:n.-155C>A
ENST00000420978.6:c.35-189C>A ENSP00000399099.2:n.35-189C>A
NM_033035.4:c.-155C>A NP_149024.1:n.-155C>A
NR_045089.1:n.1439-189C>A
NM_033035.5:c.-155C>A MANE Select NP_149024.1:n.-155C>A
NR_045089.2:n.1457-189C>A
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