Canonical Allele Identifier: CA445725896
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407672T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071974T>A , CM000667.2:g.111071974T>A GRCh38
NC_000005.9:g.110407672T>A , CM000667.1:g.110407672T>A GRCh37
NC_000005.8:g.110435571T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.84T>A MANE Select ENSP00000339804.3:p.Thr28=
ENST00000344895.3:c.84T>A ENSP00000339804.3:p.Thr28=
ENST00000420978.6:c.84T>A ENSP00000399099.2:p.Thr28=
NM_033035.4:c.84T>A NP_149024.1:p.Thr28=
NR_045089.1:n.1488T>A
NM_033035.5:c.84T>A MANE Select NP_149024.1:p.Thr28=
NR_045089.2:n.1506T>A
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