Canonical Allele Identifier: CA1080102207
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs78910837
gnomAD v3: 5-111071719-G-A
gnomAD v4: 5-111071719-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071719G>A , CM000667.2:g.111071719G>A GRCh38
NC_000005.9:g.110407417G>A , CM000667.1:g.110407417G>A GRCh37
NC_000005.8:g.110435316G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-172G>A MANE Select ENSP00000339804.3:n.-172G>A
ENST00000344895.3:c.-172G>A ENSP00000339804.3:n.-172G>A
ENST00000420978.6:c.34+202G>A ENSP00000399099.2:n.34+202G>A
NM_033035.4:c.-172G>A NP_149024.1:n.-172G>A
NR_045089.1:n.1438+202G>A
NM_033035.5:c.-172G>A MANE Select NP_149024.1:n.-172G>A
NR_045089.2:n.1456+202G>A
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