Canonical Allele Identifier: CA124873187
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs572133933
gnomAD v3: 5-111071749-G-A
gnomAD v4: 5-111071749-G-A
MyVariant Identifiers: chr5:g.110407447G>A (hg19) chr5:g.111071749G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071749G>A , CM000667.2:g.111071749G>A GRCh38
NC_000005.9:g.110407447G>A , CM000667.1:g.110407447G>A GRCh37
NC_000005.8:g.110435346G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-142G>A MANE Select ENSP00000339804.3:n.-142G>A
ENST00000344895.3:c.-142G>A ENSP00000339804.3:n.-142G>A
ENST00000420978.6:c.35-176G>A ENSP00000399099.2:n.35-176G>A
NM_033035.4:c.-142G>A NP_149024.1:n.-142G>A
NR_045089.1:n.1439-176G>A
NM_033035.5:c.-142G>A MANE Select NP_149024.1:n.-142G>A
NR_045089.2:n.1457-176G>A
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