Canonical Allele Identifier: CA561869494
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1287858056
gnomAD v2: 5-110407108-A-G
gnomAD v3: 5-111071410-A-G
gnomAD v4: 5-111071410-A-G
MyVariant Identifiers: chr5:g.110407108A>G (hg19) chr5:g.111071410A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071410A>G , CM000667.2:g.111071410A>G GRCh38
NC_000005.9:g.110407108A>G , CM000667.1:g.110407108A>G GRCh37
NC_000005.8:g.110435007A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-74A>G ENSP00000399099.2:n.-74A>G
NR_045089.1:n.1331A>G
NR_045089.2:n.1349A>G
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