Canonical Allele Identifier: CA360602403
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111071902-T-A
MyVariant Identifiers: chr5:g.110407600T>A (hg19) chr5:g.111071902T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071902T>A , CM000667.2:g.111071902T>A GRCh38
NC_000005.9:g.110407600T>A , CM000667.1:g.110407600T>A GRCh37
NC_000005.8:g.110435499T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.12T>A MANE Select ENSP00000339804.3:p.Phe4Leu
ENST00000344895.3:c.12T>A ENSP00000339804.3:p.Phe4Leu
ENST00000420978.6:c.35-23T>A ENSP00000399099.2:n.35-23T>A
NM_033035.4:c.12T>A NP_149024.1:p.Phe4Leu
NR_045089.1:n.1439-23T>A
NM_033035.5:c.12T>A MANE Select NP_149024.1:p.Phe4Leu
NR_045089.2:n.1457-23T>A
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