Canonical Allele Identifier: CA124873300
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs766846474
gnomAD v3: 5-111071850-A-G
gnomAD v4: 5-111071850-A-G
MyVariant Identifiers: chr5:g.110407548A>G (hg19) chr5:g.111071850A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071850A>G , CM000667.2:g.111071850A>G GRCh38
NC_000005.9:g.110407548A>G , CM000667.1:g.110407548A>G GRCh37
NC_000005.8:g.110435447A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-41A>G MANE Select ENSP00000339804.3:n.-41A>G
ENST00000344895.3:c.-41A>G ENSP00000339804.3:n.-41A>G
ENST00000420978.6:c.35-75A>G ENSP00000399099.2:n.35-75A>G
NM_033035.4:c.-41A>G NP_149024.1:n.-41A>G
NR_045089.1:n.1439-75A>G
NM_033035.5:c.-41A>G MANE Select NP_149024.1:n.-41A>G
NR_045089.2:n.1457-75A>G
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