Canonical Allele Identifier: CA124874221
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs374702433
gnomAD v2: 5-110408173-T-C
gnomAD v3: 5-111072475-T-C
gnomAD v4: 5-111072475-T-C
MyVariant Identifiers: chr5:g.110408173T>C (hg19) chr5:g.111072475T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072475T>C , CM000667.2:g.111072475T>C GRCh38
NC_000005.9:g.110408173T>C , CM000667.1:g.110408173T>C GRCh37
NC_000005.8:g.110436072T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.172-413T>C MANE Select ENSP00000339804.3:n.172-413T>C
ENST00000344895.3:c.172-413T>C ENSP00000339804.3:n.172-413T>C
ENST00000420978.6:c.172-413T>C ENSP00000399099.2:n.172-413T>C
NM_033035.4:c.172-413T>C NP_149024.1:n.172-413T>C
NR_045089.1:n.1576-413T>C
NM_033035.5:c.172-413T>C MANE Select NP_149024.1:n.172-413T>C
NR_045089.2:n.1594-413T>C
Search 100 bp 5'
Search 100 bp 3'