Canonical Allele Identifier: CA124872881
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs532579260
gnomAD v2: 5-110407131-C-T
gnomAD v3: 5-111071433-C-T
gnomAD v4: 5-111071433-C-T
MyVariant Identifiers: chr5:g.110407131C>T (hg19) chr5:g.111071433C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071433C>T , CM000667.2:g.111071433C>T GRCh38
NC_000005.9:g.110407131C>T , CM000667.1:g.110407131C>T GRCh37
NC_000005.8:g.110435030C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-51C>T ENSP00000399099.2:n.-51C>T
NR_045089.1:n.1354C>T
NR_045089.2:n.1372C>T
Search 100 bp 5'
Search 100 bp 3'