Canonical Allele Identifier: CA1080102300
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752360844
gnomAD v3: 5-111072256-G-A
gnomAD v4: 5-111072256-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072256G>A , CM000667.2:g.111072256G>A GRCh38
NC_000005.9:g.110407954G>A , CM000667.1:g.110407954G>A GRCh37
NC_000005.8:g.110435853G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.171+195G>A MANE Select ENSP00000339804.3:n.171+195G>A
ENST00000344895.3:c.171+195G>A ENSP00000339804.3:n.171+195G>A
ENST00000420978.6:c.171+195G>A ENSP00000399099.2:n.171+195G>A
NM_033035.4:c.171+195G>A NP_149024.1:n.171+195G>A
NR_045089.1:n.1575+195G>A
NM_033035.5:c.171+195G>A MANE Select NP_149024.1:n.171+195G>A
NR_045089.2:n.1593+195G>A
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