Canonical Allele Identifier: CA2674827599
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071551A>G , CM000667.2:g.111071551A>G GRCh38
NC_000005.9:g.110407249A>G , CM000667.1:g.110407249A>G GRCh37
NC_000005.8:g.110435148A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+34A>G ENSP00000399099.2:n.34+34A>G
NR_045089.1:n.1438+34A>G
NR_045089.2:n.1456+34A>G