Canonical Allele Identifier: CA801887561
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1268747608
gnomAD v3: 5-111072327-C-T
gnomAD v4: 5-111072327-C-T
MyVariant Identifiers: chr5:g.110408025C>T (hg19) chr5:g.111072327C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072327C>T , CM000667.2:g.111072327C>T GRCh38
NC_000005.9:g.110408025C>T , CM000667.1:g.110408025C>T GRCh37
NC_000005.8:g.110435924C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+266C>T MANE Select ENSP00000339804.3:n.171+266C>T
ENST00000344895.3:c.171+266C>T ENSP00000339804.3:n.171+266C>T
ENST00000420978.6:c.171+266C>T ENSP00000399099.2:n.171+266C>T
NM_033035.4:c.171+266C>T NP_149024.1:n.171+266C>T
NR_045089.1:n.1575+266C>T
NM_033035.5:c.171+266C>T MANE Select NP_149024.1:n.171+266C>T
NR_045089.2:n.1593+266C>T
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