Canonical Allele Identifier: CA801886749
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1360441640

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071416G>C , CM000667.2:g.111071416G>C GRCh38
NC_000005.9:g.110407114G>C , CM000667.1:g.110407114G>C GRCh37
NC_000005.8:g.110435013G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-68G>C ENSP00000399099.2:n.-68G>C
NR_045089.1:n.1337G>C
NR_045089.2:n.1355G>C