Canonical Allele Identifier: CA445725901
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111071986-T-C
MyVariant Identifiers: chr5:g.110407684T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071986T>C , CM000667.2:g.111071986T>C GRCh38
NC_000005.9:g.110407684T>C , CM000667.1:g.110407684T>C GRCh37
NC_000005.8:g.110435583T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.96T>C MANE Select ENSP00000339804.3:p.Thr32=
ENST00000344895.3:c.96T>C ENSP00000339804.3:p.Thr32=
ENST00000420978.6:c.96T>C ENSP00000399099.2:p.Thr32=
NM_033035.4:c.96T>C NP_149024.1:p.Thr32=
NR_045089.1:n.1500T>C
NM_033035.5:c.96T>C MANE Select NP_149024.1:p.Thr32=
NR_045089.2:n.1518T>C
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