Canonical Allele Identifier: CA360602422
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1290698068

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071912T>A , CM000667.2:g.111071912T>A GRCh38
NC_000005.9:g.110407610T>A , CM000667.1:g.110407610T>A GRCh37
NC_000005.8:g.110435509T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.22T>A MANE Select ENSP00000339804.3:p.Tyr8Asn
ENST00000344895.3:c.22T>A ENSP00000339804.3:p.Tyr8Asn
ENST00000420978.6:c.35-13T>A ENSP00000399099.2:n.35-13T>A
NM_033035.4:c.22T>A NP_149024.1:p.Tyr8Asn
NR_045089.1:n.1439-13T>A
NM_033035.5:c.22T>A MANE Select NP_149024.1:p.Tyr8Asn
NR_045089.2:n.1457-13T>A