Canonical Allele Identifier: CA3364847
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs377070403
ExAC: 5:110407538 C / T
gnomAD v2: 5-110407538-C-T
gnomAD v3: 5-111071840-C-T
gnomAD v4: 5-111071840-C-T
MyVariant Identifiers: chr5:g.110407538C>T (hg19) chr5:g.111071840C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071840C>T , CM000667.2:g.111071840C>T GRCh38
NC_000005.9:g.110407538C>T , CM000667.1:g.110407538C>T GRCh37
NC_000005.8:g.110435437C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-51C>T MANE Select ENSP00000339804.3:n.-51C>T
ENST00000344895.3:c.-51C>T ENSP00000339804.3:n.-51C>T
ENST00000420978.6:c.35-85C>T ENSP00000399099.2:n.35-85C>T
NM_033035.4:c.-51C>T NP_149024.1:n.-51C>T
NR_045089.1:n.1439-85C>T
NM_033035.5:c.-51C>T MANE Select NP_149024.1:n.-51C>T
NR_045089.2:n.1457-85C>T
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