Canonical Allele Identifier: CA561871815
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1162186685
gnomAD v2: 5-110413717-A-G
gnomAD v3: 5-111078019-A-G
gnomAD v4: 5-111078019-A-G
MyVariant Identifiers: chr5:g.110413717A>G (hg19) chr5:g.111078019A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111078019A>G , CM000667.2:g.111078019A>G GRCh38
NC_000005.9:g.110413717A>G , CM000667.1:g.110413717A>G GRCh37
NC_000005.8:g.110441616A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1945A>G MANE Select ENSP00000339804.3:n.*1945A>G
ENST00000379706.4:c.*1945A>G ENSP00000427827.1:n.*1945A>G
NM_033035.4:c.*1945A>G NP_149024.1:n.*1945A>G
NM_138551.4:c.*1945A>G NP_612561.2:n.*1945A>G
NR_045089.1:n.3829A>G
NM_033035.5:c.*1945A>G MANE Select NP_149024.1:n.*1945A>G
NM_138551.5:c.*1945A>G NP_612561.2:n.*1945A>G
NR_045089.2:n.3847A>G
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