Canonical Allele Identifier: CA1572617375
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1580375741
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072497T>C , CM000667.2:g.111072497T>C GRCh38
NC_000005.9:g.110408195T>C , CM000667.1:g.110408195T>C GRCh37
NC_000005.8:g.110436094T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-391T>C MANE Select ENSP00000339804.3:n.172-391T>C
ENST00000344895.3:c.172-391T>C ENSP00000339804.3:n.172-391T>C
ENST00000420978.6:c.172-391T>C ENSP00000399099.2:n.172-391T>C
NM_033035.4:c.172-391T>C NP_149024.1:n.172-391T>C
NR_045089.1:n.1576-391T>C
NM_033035.5:c.172-391T>C MANE Select NP_149024.1:n.172-391T>C
NR_045089.2:n.1594-391T>C
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