Canonical Allele Identifier: CA801857100

Gene: TSLP

Linked Data

• dbSNP Id: rs1230095722
• MyVariant Identifiers: chr5:g.110413650T>A (hg19) ; chr5:g.111077952T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111077952T>A , CM000667.2:g.111077952T>A	GRCh38
NC_000005.9:g.110413650T>A , CM000667.1:g.110413650T>A	GRCh37
NC_000005.8:g.110441549T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000344895.4:c.*1878T>A MANE Select	ENSP00000339804.3:n.*1878T>A
ENST00000379706.4:c.*1878T>A	ENSP00000427827.1:n.*1878T>A
NM_033035.4:c.*1878T>A	NP_149024.1:n.*1878T>A
NM_138551.4:c.*1878T>A	NP_612561.2:n.*1878T>A
NR_045089.1:n.3762T>A
NM_033035.5:c.*1878T>A MANE Select	NP_149024.1:n.*1878T>A
NM_138551.5:c.*1878T>A	NP_612561.2:n.*1878T>A
NR_045089.2:n.3780T>A