Canonical Allele Identifier: CA801887016
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1225473986

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071825C>G , CM000667.2:g.111071825C>G GRCh38
NC_000005.9:g.110407523C>G , CM000667.1:g.110407523C>G GRCh37
NC_000005.8:g.110435422C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.-66C>G MANE Select ENSP00000339804.3:n.-66C>G
ENST00000344895.3:c.-66C>G ENSP00000339804.3:n.-66C>G
ENST00000420978.6:c.35-100C>G ENSP00000399099.2:n.35-100C>G
NM_033035.4:c.-66C>G NP_149024.1:n.-66C>G
NR_045089.1:n.1439-100C>G
NM_033035.5:c.-66C>G MANE Select NP_149024.1:n.-66C>G
NR_045089.2:n.1457-100C>G