Canonical Allele Identifier: CA2674827814
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071802A>T , CM000667.2:g.111071802A>T GRCh38
NC_000005.9:g.110407500A>T , CM000667.1:g.110407500A>T GRCh37
NC_000005.8:g.110435399A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-89A>T MANE Select ENSP00000339804.3:n.-89A>T
ENST00000344895.3:c.-89A>T ENSP00000339804.3:n.-89A>T
ENST00000420978.6:c.35-123A>T ENSP00000399099.2:n.35-123A>T
NM_033035.4:c.-89A>T NP_149024.1:n.-89A>T
NR_045089.1:n.1439-123A>T
NM_033035.5:c.-89A>T MANE Select NP_149024.1:n.-89A>T
NR_045089.2:n.1457-123A>T