Canonical Allele Identifier: CA360602500
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407647T>C (hg19) chr5:g.111071949T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071949T>C , CM000667.2:g.111071949T>C GRCh38
NC_000005.9:g.110407647T>C , CM000667.1:g.110407647T>C GRCh37
NC_000005.8:g.110435546T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.59T>C MANE Select ENSP00000339804.3:p.Leu20Ser
ENST00000344895.3:c.59T>C ENSP00000339804.3:p.Leu20Ser
ENST00000420978.6:c.59T>C ENSP00000399099.2:p.Leu20Ser
NM_033035.4:c.59T>C NP_149024.1:p.Leu20Ser
NR_045089.1:n.1463T>C
NM_033035.5:c.59T>C MANE Select NP_149024.1:p.Leu20Ser
NR_045089.2:n.1481T>C
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