Canonical Allele Identifier: CA2556917862
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071750A>G , CM000667.2:g.111071750A>G GRCh38
NC_000005.9:g.110407448A>G , CM000667.1:g.110407448A>G GRCh37
NC_000005.8:g.110435347A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-141A>G MANE Select ENSP00000339804.3:n.-141A>G
ENST00000344895.3:c.-141A>G ENSP00000339804.3:n.-141A>G
ENST00000420978.6:c.35-175A>G ENSP00000399099.2:n.35-175A>G
NM_033035.4:c.-141A>G NP_149024.1:n.-141A>G
NR_045089.1:n.1439-175A>G
NM_033035.5:c.-141A>G MANE Select NP_149024.1:n.-141A>G
NR_045089.2:n.1457-175A>G