Canonical Allele Identifier: CA360602431
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407614T>A (hg19) chr5:g.111071916T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071916T>A , CM000667.2:g.111071916T>A GRCh38
NC_000005.9:g.110407614T>A , CM000667.1:g.110407614T>A GRCh37
NC_000005.8:g.110435513T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.26T>A MANE Select ENSP00000339804.3:p.Val9Asp
ENST00000344895.3:c.26T>A ENSP00000339804.3:p.Val9Asp
ENST00000420978.6:c.35-9T>A ENSP00000399099.2:n.35-9T>A
NM_033035.4:c.26T>A NP_149024.1:p.Val9Asp
NR_045089.1:n.1439-9T>A
NM_033035.5:c.26T>A MANE Select NP_149024.1:p.Val9Asp
NR_045089.2:n.1457-9T>A
Search 100 bp 5'
Search 100 bp 3'