Canonical Allele Identifier: CA124879435
Gene: TSLP HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.111076887A>G
GRCh37 chr5:g.110412585A>G
gnomAD v2:
5:110412585 A / G
gnomAD v3:
5:111076887 A / G
gnomAD v4:
chr5-111076887-A-G
Joint Max Group AF 0.26624302 (SAS)
Genomes Max Group AF 0.26624302 (SAS)
Exomes Max Group AF 0.06814 (NFE)
dbSNP:
11466749
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111076887A>G , CM000667.2:g.111076887A>G GRCh38
NC_000005.9:g.110412585A>G , CM000667.1:g.110412585A>G GRCh37
NC_000005.8:g.110440484A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*813A>G MANE Select ENSP00000339804.3:n.*813A>G
ENST00000379706.4:c.*813A>G ENSP00000427827.1:n.*813A>G
NM_033035.4:c.*813A>G NP_149024.1:n.*813A>G
NM_138551.4:c.*813A>G NP_612561.2:n.*813A>G
NR_045089.1:n.2697A>G
NM_033035.5:c.*813A>G MANE Select NP_149024.1:n.*813A>G
NM_138551.5:c.*813A>G NP_612561.2:n.*813A>G
NR_045089.2:n.2715A>G
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