Canonical Allele Identifier: CA561871445
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1237489463
gnomAD v2: 5-110412962-A-C
gnomAD v3: 5-111077264-A-C
gnomAD v4: 5-111077264-A-C
MyVariant Identifiers: chr5:g.110412962A>C (hg19) chr5:g.111077264A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077264A>C , CM000667.2:g.111077264A>C GRCh38
NC_000005.9:g.110412962A>C , CM000667.1:g.110412962A>C GRCh37
NC_000005.8:g.110440861A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1190A>C MANE Select ENSP00000339804.3:n.*1190A>C
ENST00000379706.4:c.*1190A>C ENSP00000427827.1:n.*1190A>C
NM_033035.4:c.*1190A>C NP_149024.1:n.*1190A>C
NM_138551.4:c.*1190A>C NP_612561.2:n.*1190A>C
NR_045089.1:n.3074A>C
NM_033035.5:c.*1190A>C MANE Select NP_149024.1:n.*1190A>C
NM_138551.5:c.*1190A>C NP_612561.2:n.*1190A>C
NR_045089.2:n.3092A>C
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