Canonical Allele Identifier: CA3364852
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs769818116
ExAC: 5:110407564 C / A
gnomAD v2: 5-110407564-C-A
MyVariant Identifiers: chr5:g.110407564C>A (hg19) chr5:g.111071866C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071866C>A , CM000667.2:g.111071866C>A GRCh38
NC_000005.9:g.110407564C>A , CM000667.1:g.110407564C>A GRCh37
NC_000005.8:g.110435463C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-25C>A MANE Select ENSP00000339804.3:n.-25C>A
ENST00000344895.3:c.-25C>A ENSP00000339804.3:n.-25C>A
ENST00000420978.6:c.35-59C>A ENSP00000399099.2:n.35-59C>A
NM_033035.4:c.-25C>A NP_149024.1:n.-25C>A
NR_045089.1:n.1439-59C>A
NM_033035.5:c.-25C>A MANE Select NP_149024.1:n.-25C>A
NR_045089.2:n.1457-59C>A
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