Canonical Allele Identifier: CA360602407
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407602C>A (hg19) chr5:g.111071904C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071904C>A , CM000667.2:g.111071904C>A GRCh38
NC_000005.9:g.110407602C>A , CM000667.1:g.110407602C>A GRCh37
NC_000005.8:g.110435501C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.14C>A MANE Select ENSP00000339804.3:p.Ala5Asp
ENST00000344895.3:c.14C>A ENSP00000339804.3:p.Ala5Asp
ENST00000420978.6:c.35-21C>A ENSP00000399099.2:n.35-21C>A
NM_033035.4:c.14C>A NP_149024.1:p.Ala5Asp
NR_045089.1:n.1439-21C>A
NM_033035.5:c.14C>A MANE Select NP_149024.1:p.Ala5Asp
NR_045089.2:n.1457-21C>A
Search 100 bp 5'
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