Canonical Allele Identifier: CA1572616547
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752343159
gnomAD v4: 5-111071814-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071814G>A , CM000667.2:g.111071814G>A GRCh38
NC_000005.9:g.110407512G>A , CM000667.1:g.110407512G>A GRCh37
NC_000005.8:g.110435411G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.-77G>A MANE Select ENSP00000339804.3:n.-77G>A
ENST00000344895.3:c.-77G>A ENSP00000339804.3:n.-77G>A
ENST00000420978.6:c.35-111G>A ENSP00000399099.2:n.35-111G>A
NM_033035.4:c.-77G>A NP_149024.1:n.-77G>A
NR_045089.1:n.1439-111G>A
NM_033035.5:c.-77G>A MANE Select NP_149024.1:n.-77G>A
NR_045089.2:n.1457-111G>A
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