Canonical Allele Identifier: CA3364857
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs771325593
ExAC: 5:110407586 CG / C
gnomAD v2: 5-110407586-CG-C
gnomAD v3: 5-111071888-CG-C
gnomAD v4: 5-111071888-CG-C
MyVariant Identifiers: chr5:g.110407587del (hg19) chr5:g.111071889del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071889del , CM000667.2:g.111071889del GRCh38
NC_000005.9:g.110407587del , CM000667.1:g.110407587del GRCh37
NC_000005.8:g.110435486del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-2del MANE Select ENSP00000339804.3:n.-2del
ENST00000344895.3:c.-2del ENSP00000339804.3:n.-2del
ENST00000420978.6:c.35-36del ENSP00000399099.2:n.35-36del
NM_033035.4:c.-2del NP_149024.1:n.-2del
NR_045089.1:n.1439-36del
NM_033035.5:c.-2del MANE Select NP_149024.1:n.-2del
NR_045089.2:n.1457-36del
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