Canonical Allele Identifier: CA1572622509
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752532549
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077129C>T , CM000667.2:g.111077129C>T GRCh38
NC_000005.9:g.110412827C>T , CM000667.1:g.110412827C>T GRCh37
NC_000005.8:g.110440726C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1055C>T MANE Select ENSP00000339804.3:n.*1055C>T
ENST00000379706.4:c.*1055C>T ENSP00000427827.1:n.*1055C>T
NM_033035.4:c.*1055C>T NP_149024.1:n.*1055C>T
NM_138551.4:c.*1055C>T NP_612561.2:n.*1055C>T
NR_045089.1:n.2939C>T
NM_033035.5:c.*1055C>T MANE Select NP_149024.1:n.*1055C>T
NM_138551.5:c.*1055C>T NP_612561.2:n.*1055C>T
NR_045089.2:n.2957C>T
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