Canonical Allele Identifier: CA1572616560
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1561690243

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071826A>G , CM000667.2:g.111071826A>G GRCh38
NC_000005.9:g.110407524A>G , CM000667.1:g.110407524A>G GRCh37
NC_000005.8:g.110435423A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.-65A>G MANE Select ENSP00000339804.3:n.-65A>G
ENST00000344895.3:c.-65A>G ENSP00000339804.3:n.-65A>G
ENST00000420978.6:c.35-99A>G ENSP00000399099.2:n.35-99A>G
NM_033035.4:c.-65A>G NP_149024.1:n.-65A>G
NR_045089.1:n.1439-99A>G
NM_033035.5:c.-65A>G MANE Select NP_149024.1:n.-65A>G
NR_045089.2:n.1457-99A>G