Canonical Allele Identifier: CA561869612

Gene: TSLP

Linked Data

• dbSNP Id: rs1184501056
• gnomAD v2: 5-110407972-G-A
• gnomAD v3: 5-111072274-G-A
• gnomAD v4: 5-111072274-G-A
• MyVariant Identifiers: chr5:g.110407972G>A (hg19) ; chr5:g.111072274G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111072274G>A , CM000667.2:g.111072274G>A	GRCh38
NC_000005.9:g.110407972G>A , CM000667.1:g.110407972G>A	GRCh37
NC_000005.8:g.110435871G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.171+213G>A MANE Select	ENSP00000339804.3:n.171+213G>A
ENST00000344895.3:c.171+213G>A	ENSP00000339804.3:n.171+213G>A
ENST00000420978.6:c.171+213G>A	ENSP00000399099.2:n.171+213G>A
NM_033035.4:c.171+213G>A	NP_149024.1:n.171+213G>A
NR_045089.1:n.1575+213G>A
NM_033035.5:c.171+213G>A MANE Select	NP_149024.1:n.171+213G>A
NR_045089.2:n.1593+213G>A