Canonical Allele Identifier: CA360602297
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1452628128
gnomAD v2: 5-110407186-A-G
gnomAD v3: 5-111071488-A-G
gnomAD v4: 5-111071488-A-G
MyVariant Identifiers: chr5:g.110407186A>G (hg19) chr5:g.111071488A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071488A>G , CM000667.2:g.111071488A>G GRCh38
NC_000005.9:g.110407186A>G , CM000667.1:g.110407186A>G GRCh37
NC_000005.8:g.110435085A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.5A>G ENSP00000399099.2:p.Lys2Arg
NR_045089.1:n.1409A>G
NR_045089.2:n.1427A>G
Search 100 bp 5'
Search 100 bp 3'