Canonical Allele Identifier: CA124880731
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs772764272
gnomAD v2: 5-110413713-T-C
gnomAD v3: 5-111078015-T-C
gnomAD v4: 5-111078015-T-C
MyVariant Identifiers: chr5:g.110413713T>C (hg19) chr5:g.111078015T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111078015T>C , CM000667.2:g.111078015T>C GRCh38
NC_000005.9:g.110413713T>C , CM000667.1:g.110413713T>C GRCh37
NC_000005.8:g.110441612T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1941T>C MANE Select ENSP00000339804.3:n.*1941T>C
ENST00000379706.4:c.*1941T>C ENSP00000427827.1:n.*1941T>C
NM_033035.4:c.*1941T>C NP_149024.1:n.*1941T>C
NM_138551.4:c.*1941T>C NP_612561.2:n.*1941T>C
NR_045089.1:n.3825T>C
NM_033035.5:c.*1941T>C MANE Select NP_149024.1:n.*1941T>C
NM_138551.5:c.*1941T>C NP_612561.2:n.*1941T>C
NR_045089.2:n.3843T>C
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