Canonical Allele Identifier: CA124880673

Gene: TSLP

Linked Data

• dbSNP Id: rs758926265
• gnomAD v2: 5-110413671-C-A
• gnomAD v3: 5-111077973-C-A
• gnomAD v4: 5-111077973-C-A
• MyVariant Identifiers: chr5:g.110413671C>A (hg19) ; chr5:g.111077973C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111077973C>A , CM000667.2:g.111077973C>A	GRCh38
NC_000005.9:g.110413671C>A , CM000667.1:g.110413671C>A	GRCh37
NC_000005.8:g.110441570C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000344895.4:c.*1899C>A MANE Select	ENSP00000339804.3:n.*1899C>A
ENST00000379706.4:c.*1899C>A	ENSP00000427827.1:n.*1899C>A
NM_033035.4:c.*1899C>A	NP_149024.1:n.*1899C>A
NM_138551.4:c.*1899C>A	NP_612561.2:n.*1899C>A
NR_045089.1:n.3783C>A
NM_033035.5:c.*1899C>A MANE Select	NP_149024.1:n.*1899C>A
NM_138551.5:c.*1899C>A	NP_612561.2:n.*1899C>A
NR_045089.2:n.3801C>A