Canonical Allele Identifier: CA2674827784
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111071772-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071772G>A , CM000667.2:g.111071772G>A GRCh38
NC_000005.9:g.110407470G>A , CM000667.1:g.110407470G>A GRCh37
NC_000005.8:g.110435369G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-119G>A MANE Select ENSP00000339804.3:n.-119G>A
ENST00000344895.3:c.-119G>A ENSP00000339804.3:n.-119G>A
ENST00000420978.6:c.35-153G>A ENSP00000399099.2:n.35-153G>A
NM_033035.4:c.-119G>A NP_149024.1:n.-119G>A
NR_045089.1:n.1439-153G>A
NM_033035.5:c.-119G>A MANE Select NP_149024.1:n.-119G>A
NR_045089.2:n.1457-153G>A
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