Canonical Allele Identifier: CA2674827800
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071790T>G , CM000667.2:g.111071790T>G GRCh38
NC_000005.9:g.110407488T>G , CM000667.1:g.110407488T>G GRCh37
NC_000005.8:g.110435387T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-101T>G MANE Select ENSP00000339804.3:n.-101T>G
ENST00000344895.3:c.-101T>G ENSP00000339804.3:n.-101T>G
ENST00000420978.6:c.35-135T>G ENSP00000399099.2:n.35-135T>G
NM_033035.4:c.-101T>G NP_149024.1:n.-101T>G
NR_045089.1:n.1439-135T>G
NM_033035.5:c.-101T>G MANE Select NP_149024.1:n.-101T>G
NR_045089.2:n.1457-135T>G