Canonical Allele Identifier: CA445725890
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407666G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071968G>C , CM000667.2:g.111071968G>C GRCh38
NC_000005.9:g.110407666G>C , CM000667.1:g.110407666G>C GRCh37
NC_000005.8:g.110435565G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.78G>C MANE Select ENSP00000339804.3:p.Val26=
ENST00000344895.3:c.78G>C ENSP00000339804.3:p.Val26=
ENST00000420978.6:c.78G>C ENSP00000399099.2:p.Val26=
NM_033035.4:c.78G>C NP_149024.1:p.Val26=
NR_045089.1:n.1482G>C
NM_033035.5:c.78G>C MANE Select NP_149024.1:p.Val26=
NR_045089.2:n.1500G>C
Search 100 bp 5'
Search 100 bp 3'