Canonical Allele Identifier: CA1080102241
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752345546

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071890T>A , CM000667.2:g.111071890T>A GRCh38
NC_000005.9:g.110407588T>A , CM000667.1:g.110407588T>A GRCh37
NC_000005.8:g.110435487T>A NCBI36

Transcript Alleles

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