Canonical Allele Identifier: CA801886877
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1307298699
MyVariant Identifiers: chr5:g.110407219A>C (hg19) chr5:g.111071521A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071521A>C , CM000667.2:g.111071521A>C GRCh38
NC_000005.9:g.110407219A>C , CM000667.1:g.110407219A>C GRCh37
NC_000005.8:g.110435118A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+4A>C ENSP00000399099.2:n.34+4A>C
NR_045089.1:n.1438+4A>C
NR_045089.2:n.1456+4A>C
Search 100 bp 5'
Search 100 bp 3'