Canonical Allele Identifier: CA2674827949
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111072204-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072204G>T , CM000667.2:g.111072204G>T GRCh38
NC_000005.9:g.110407902G>T , CM000667.1:g.110407902G>T GRCh37
NC_000005.8:g.110435801G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.171+143G>T MANE Select ENSP00000339804.3:n.171+143G>T
ENST00000344895.3:c.171+143G>T ENSP00000339804.3:n.171+143G>T
ENST00000420978.6:c.171+143G>T ENSP00000399099.2:n.171+143G>T
NM_033035.4:c.171+143G>T NP_149024.1:n.171+143G>T
NR_045089.1:n.1575+143G>T
NM_033035.5:c.171+143G>T MANE Select NP_149024.1:n.171+143G>T
NR_045089.2:n.1593+143G>T
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