Canonical Allele Identifier: CA1572617352
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752366257
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072468A>G , CM000667.2:g.111072468A>G GRCh38
NC_000005.9:g.110408166A>G , CM000667.1:g.110408166A>G GRCh37
NC_000005.8:g.110436065A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+407A>G MANE Select ENSP00000339804.3:n.171+407A>G
ENST00000344895.3:c.171+407A>G ENSP00000339804.3:n.171+407A>G
ENST00000420978.6:c.171+407A>G ENSP00000399099.2:n.171+407A>G
NM_033035.4:c.171+407A>G NP_149024.1:n.171+407A>G
NR_045089.1:n.1575+407A>G
NM_033035.5:c.171+407A>G MANE Select NP_149024.1:n.171+407A>G
NR_045089.2:n.1593+407A>G
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