Canonical Allele Identifier: CA1572622493
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1580379416
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077119G>A , CM000667.2:g.111077119G>A GRCh38
NC_000005.9:g.110412817G>A , CM000667.1:g.110412817G>A GRCh37
NC_000005.8:g.110440716G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1045G>A MANE Select ENSP00000339804.3:n.*1045G>A
ENST00000379706.4:c.*1045G>A ENSP00000427827.1:n.*1045G>A
NM_033035.4:c.*1045G>A NP_149024.1:n.*1045G>A
NM_138551.4:c.*1045G>A NP_612561.2:n.*1045G>A
NR_045089.1:n.2929G>A
NM_033035.5:c.*1045G>A MANE Select NP_149024.1:n.*1045G>A
NM_138551.5:c.*1045G>A NP_612561.2:n.*1045G>A
NR_045089.2:n.2947G>A
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