Canonical Allele Identifier: CA2674827769
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071755G>T , CM000667.2:g.111071755G>T GRCh38
NC_000005.9:g.110407453G>T , CM000667.1:g.110407453G>T GRCh37
NC_000005.8:g.110435352G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-136G>T MANE Select ENSP00000339804.3:n.-136G>T
ENST00000344895.3:c.-136G>T ENSP00000339804.3:n.-136G>T
ENST00000420978.6:c.35-170G>T ENSP00000399099.2:n.35-170G>T
NM_033035.4:c.-136G>T NP_149024.1:n.-136G>T
NR_045089.1:n.1439-170G>T
NM_033035.5:c.-136G>T MANE Select NP_149024.1:n.-136G>T
NR_045089.2:n.1457-170G>T