Canonical Allele Identifier: CA562217229
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1407171511

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071822T>G , CM000667.2:g.111071822T>G GRCh38
NC_000005.9:g.110407520T>G , CM000667.1:g.110407520T>G GRCh37
NC_000005.8:g.110435419T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.-69T>G MANE Select ENSP00000339804.3:n.-69T>G
ENST00000344895.3:c.-69T>G ENSP00000339804.3:n.-69T>G
ENST00000420978.6:c.35-103T>G ENSP00000399099.2:n.35-103T>G
NM_033035.4:c.-69T>G NP_149024.1:n.-69T>G
NR_045089.1:n.1439-103T>G
NM_033035.5:c.-69T>G MANE Select NP_149024.1:n.-69T>G
NR_045089.2:n.1457-103T>G