Canonical Allele Identifier: CA915184198
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1561693093

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077112A>T , CM000667.2:g.111077112A>T GRCh38
NC_000005.9:g.110412810A>T , CM000667.1:g.110412810A>T GRCh37
NC_000005.8:g.110440709A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1038A>T MANE Select ENSP00000339804.3:n.*1038A>T
ENST00000379706.4:c.*1038A>T ENSP00000427827.1:n.*1038A>T
NM_033035.4:c.*1038A>T NP_149024.1:n.*1038A>T
NM_138551.4:c.*1038A>T NP_612561.2:n.*1038A>T
NR_045089.1:n.2922A>T
NM_033035.5:c.*1038A>T MANE Select NP_149024.1:n.*1038A>T
NM_138551.5:c.*1038A>T NP_612561.2:n.*1038A>T
NR_045089.2:n.2940A>T