Canonical Allele Identifier: CA2578376657
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071840C>G , CM000667.2:g.111071840C>G GRCh38
NC_000005.9:g.110407538C>G , CM000667.1:g.110407538C>G GRCh37
NC_000005.8:g.110435437C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-51C>G MANE Select ENSP00000339804.3:n.-51C>G
ENST00000344895.3:c.-51C>G ENSP00000339804.3:n.-51C>G
ENST00000420978.6:c.35-85C>G ENSP00000399099.2:n.35-85C>G
NM_033035.4:c.-51C>G NP_149024.1:n.-51C>G
NR_045089.1:n.1439-85C>G
NM_033035.5:c.-51C>G MANE Select NP_149024.1:n.-51C>G
NR_045089.2:n.1457-85C>G