Canonical Allele Identifier: CA2832184629
Gene: TSLP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072470G>A , CM000667.2:g.111072470G>A GRCh38
NC_000005.9:g.110408168G>A , CM000667.1:g.110408168G>A GRCh37
NC_000005.8:g.110436067G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+409G>A MANE Select ENSP00000339804.3:n.171+409G>A
ENST00000344895.3:c.171+409G>A ENSP00000339804.3:n.171+409G>A
ENST00000420978.6:c.171+409G>A ENSP00000399099.2:n.171+409G>A
NM_033035.4:c.171+409G>A NP_149024.1:n.171+409G>A
NR_045089.1:n.1575+409G>A
NM_033035.5:c.171+409G>A MANE Select NP_149024.1:n.171+409G>A
NR_045089.2:n.1593+409G>A
Search 100 bp 5'
Search 100 bp 3'