Canonical Allele Identifier: CA12103925
Gene: TSLP HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.111071809C>T
GRCh37 chr5:g.110407507C>T
gnomAD v2:
5:110407507 C / T
gnomAD v3:
5:111071809 C / T
gnomAD v4:
chr5-111071809-C-T
Joint Max Group AF 0.3937019 (MID)
Genomes Max Group AF 0.37022523 (SAS)
Exomes Max Group AF 0.40171892 (AMR)
dbSNP:
2289276
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071809C>T , CM000667.2:g.111071809C>T GRCh38
NC_000005.9:g.110407507C>T , CM000667.1:g.110407507C>T GRCh37
NC_000005.8:g.110435406C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-82C>T MANE Select ENSP00000339804.3:n.-82C>T
ENST00000344895.3:c.-82C>T ENSP00000339804.3:n.-82C>T
ENST00000420978.6:c.35-116C>T ENSP00000399099.2:n.35-116C>T
NM_033035.4:c.-82C>T NP_149024.1:n.-82C>T
NR_045089.1:n.1439-116C>T
NM_033035.5:c.-82C>T MANE Select NP_149024.1:n.-82C>T
NR_045089.2:n.1457-116C>T
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