Canonical Allele Identifier: CA360602473
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1275574034

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071937A>G , CM000667.2:g.111071937A>G GRCh38
NC_000005.9:g.110407635A>G , CM000667.1:g.110407635A>G GRCh37
NC_000005.8:g.110435534A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.47A>G MANE Select ENSP00000339804.3:p.Lys16Arg
ENST00000344895.3:c.47A>G ENSP00000339804.3:p.Lys16Arg
ENST00000420978.6:c.47A>G ENSP00000399099.2:p.Lys16Arg
NM_033035.4:c.47A>G NP_149024.1:p.Lys16Arg
NR_045089.1:n.1451A>G
NM_033035.5:c.47A>G MANE Select NP_149024.1:p.Lys16Arg
NR_045089.2:n.1469A>G