Canonical Allele Identifier: CA801886933
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1332373049
MyVariant Identifiers: chr5:g.110407309_110407312del (hg19) chr5:g.111071611_111071614del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071612_111071615del , CM000667.2:g.111071612_111071615del GRCh38
NC_000005.9:g.110407310_110407313del , CM000667.1:g.110407310_110407313del GRCh37
NC_000005.8:g.110435209_110435212del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+95_34+98del ENSP00000399099.2:n.34+95_34+98del
NR_045089.1:n.1438+95_1438+98del
NR_045089.2:n.1456+95_1456+98del
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