Canonical Allele Identifier: CA3364861
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs760433790
ExAC: 5:110407594 C / T
gnomAD v2: 5-110407594-C-T
gnomAD v3: 5-111071896-C-T
gnomAD v4: 5-111071896-C-T
COSMIC: COSM3607502
MyVariant Identifiers: chr5:g.110407594C>T (hg19) chr5:g.111071896C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071896C>T , CM000667.2:g.111071896C>T GRCh38
NC_000005.9:g.110407594C>T , CM000667.1:g.110407594C>T GRCh37
NC_000005.8:g.110435493C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.6C>T MANE Select ENSP00000339804.3:p.Phe2=
ENST00000344895.3:c.6C>T ENSP00000339804.3:p.Phe2=
ENST00000420978.6:c.35-29C>T ENSP00000399099.2:n.35-29C>T
NM_033035.4:c.6C>T NP_149024.1:p.Phe2=
NR_045089.1:n.1439-29C>T
NM_033035.5:c.6C>T MANE Select NP_149024.1:p.Phe2=
NR_045089.2:n.1457-29C>T
Search 100 bp 5'
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