Canonical Allele Identifier: CA561869530

Gene: TSLP

Linked Data

• dbSNP Id: rs1473796600
• gnomAD v2: 5-110407202-C-T
• gnomAD v4: 5-111071504-C-T
• MyVariant Identifiers: chr5:g.110407202C>T (hg19) ; chr5:g.111071504C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111071504C>T , CM000667.2:g.111071504C>T	GRCh38
NC_000005.9:g.110407202C>T , CM000667.1:g.110407202C>T	GRCh37
NC_000005.8:g.110435101C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420978.6:c.21C>T	ENSP00000399099.2:p.Ser7=
NR_045089.1:n.1425C>T
NR_045089.2:n.1443C>T