Canonical Allele Identifier: CA124874248

Gene: TSLP

Linked Data

• dbSNP Id: rs909258630
• MyVariant Identifiers: chr5:g.110408194T>C (hg19) ; chr5:g.111072496T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111072496T>C , CM000667.2:g.111072496T>C	GRCh38
NC_000005.9:g.110408194T>C , CM000667.1:g.110408194T>C	GRCh37
NC_000005.8:g.110436093T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.172-392T>C MANE Select	ENSP00000339804.3:n.172-392T>C
ENST00000344895.3:c.172-392T>C	ENSP00000339804.3:n.172-392T>C
ENST00000420978.6:c.172-392T>C	ENSP00000399099.2:n.172-392T>C
NM_033035.4:c.172-392T>C	NP_149024.1:n.172-392T>C
NR_045089.1:n.1576-392T>C
NM_033035.5:c.172-392T>C MANE Select	NP_149024.1:n.172-392T>C
NR_045089.2:n.1594-392T>C