Canonical Allele Identifier: CA124879837
Gene: TSLP HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.111077196G>A
GRCh37 chr5:g.110412894G>A
gnomAD v2:
5:110412894 G / A
gnomAD v3:
5:111077196 G / A
gnomAD v4:
chr5-111077196-G-A
Joint Max Group AF 0.26576264 (SAS)
Genomes Max Group AF 0.2658732 (SAS)
Exomes Max Group AF 0.08884008 (AFR)
dbSNP:
11466750
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077196G>A , CM000667.2:g.111077196G>A GRCh38
NC_000005.9:g.110412894G>A , CM000667.1:g.110412894G>A GRCh37
NC_000005.8:g.110440793G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1122G>A MANE Select ENSP00000339804.3:n.*1122G>A
ENST00000379706.4:c.*1122G>A ENSP00000427827.1:n.*1122G>A
NM_033035.4:c.*1122G>A NP_149024.1:n.*1122G>A
NM_138551.4:c.*1122G>A NP_612561.2:n.*1122G>A
NR_045089.1:n.3006G>A
NM_033035.5:c.*1122G>A MANE Select NP_149024.1:n.*1122G>A
NM_138551.5:c.*1122G>A NP_612561.2:n.*1122G>A
NR_045089.2:n.3024G>A
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