Canonical Allele Identifier: CA124873408
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs570028217
gnomAD v4: 5-111071888-C-T
COSMIC: COSN8952865
MyVariant Identifiers: chr5:g.111071888C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071888C>T , CM000667.2:g.111071888C>T GRCh38
NC_000005.9:g.110407586C>T , CM000667.1:g.110407586C>T GRCh37
NC_000005.8:g.110435485C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-3C>T MANE Select ENSP00000339804.3:n.-3C>T
ENST00000344895.3:c.-3C>T ENSP00000339804.3:n.-3C>T
ENST00000420978.6:c.35-37C>T ENSP00000399099.2:n.35-37C>T
NM_033035.4:c.-3C>T NP_149024.1:n.-3C>T
NR_045089.1:n.1439-37C>T
NM_033035.5:c.-3C>T MANE Select NP_149024.1:n.-3C>T
NR_045089.2:n.1457-37C>T
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