Canonical Allele Identifier: CA3364855
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs368315454

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071882T>C , CM000667.2:g.111071882T>C GRCh38
NC_000005.9:g.110407580T>C , CM000667.1:g.110407580T>C GRCh37
NC_000005.8:g.110435479T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-9T>C MANE Select ENSP00000339804.3:n.-9T>C
ENST00000344895.3:c.-9T>C ENSP00000339804.3:n.-9T>C
ENST00000420978.6:c.35-43T>C ENSP00000399099.2:n.35-43T>C
NM_033035.4:c.-9T>C NP_149024.1:n.-9T>C
NR_045089.1:n.1439-43T>C
NM_033035.5:c.-9T>C MANE Select NP_149024.1:n.-9T>C
NR_045089.2:n.1457-43T>C