Canonical Allele Identifier: CA801887501
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1387963101
gnomAD v3: 5-111072215-A-G
gnomAD v4: 5-111072215-A-G
MyVariant Identifiers: chr5:g.110407913A>G (hg19) chr5:g.111072215A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072215A>G , CM000667.2:g.111072215A>G GRCh38
NC_000005.9:g.110407913A>G , CM000667.1:g.110407913A>G GRCh37
NC_000005.8:g.110435812A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.171+154A>G MANE Select ENSP00000339804.3:n.171+154A>G
ENST00000344895.3:c.171+154A>G ENSP00000339804.3:n.171+154A>G
ENST00000420978.6:c.171+154A>G ENSP00000399099.2:n.171+154A>G
NM_033035.4:c.171+154A>G NP_149024.1:n.171+154A>G
NR_045089.1:n.1575+154A>G
NM_033035.5:c.171+154A>G MANE Select NP_149024.1:n.171+154A>G
NR_045089.2:n.1593+154A>G
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