Canonical Allele Identifier: CA1572623236
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752555456
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077867T>C , CM000667.2:g.111077867T>C GRCh38
NC_000005.9:g.110413565T>C , CM000667.1:g.110413565T>C GRCh37
NC_000005.8:g.110441464T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1793T>C MANE Select ENSP00000339804.3:n.*1793T>C
ENST00000379706.4:c.*1793T>C ENSP00000427827.1:n.*1793T>C
NM_033035.4:c.*1793T>C NP_149024.1:n.*1793T>C
NM_138551.4:c.*1793T>C NP_612561.2:n.*1793T>C
NR_045089.1:n.3677T>C
NM_033035.5:c.*1793T>C MANE Select NP_149024.1:n.*1793T>C
NM_138551.5:c.*1793T>C NP_612561.2:n.*1793T>C
NR_045089.2:n.3695T>C
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