Canonical Allele Identifier: CA2767908743
Gene: TSLP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111078023G>C , CM000667.2:g.111078023G>C GRCh38
NC_000005.9:g.110413721G>C , CM000667.1:g.110413721G>C GRCh37
NC_000005.8:g.110441620G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1949G>C MANE Select ENSP00000339804.3:n.*1949G>C
ENST00000379706.4:c.*1949G>C ENSP00000427827.1:n.*1949G>C
NM_033035.4:c.*1949G>C NP_149024.1:n.*1949G>C
NM_138551.4:c.*1949G>C NP_612561.2:n.*1949G>C
NR_045089.1:n.3833G>C
NM_033035.5:c.*1949G>C MANE Select NP_149024.1:n.*1949G>C
NM_138551.5:c.*1949G>C NP_612561.2:n.*1949G>C
NR_045089.2:n.3851G>C
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