Canonical Allele Identifier: CA801886128

Gene: TSLP

Linked Data

• dbSNP Id: rs1431992838
• gnomAD v3: 5-111070080-A-C
• gnomAD v4: 5-111070080-A-C
• MyVariant Identifiers: chr5:g.110405778A>C (hg19) ; chr5:g.111070080A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111070080A>C , CM000667.2:g.111070080A>C	GRCh38
NC_000005.9:g.110405778A>C , CM000667.1:g.110405778A>C	GRCh37
NC_000005.8:g.110433677A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420978.6:c.-1404A>C	ENSP00000399099.2:n.-1404A>C
NR_045089.1:n.1A>C
NR_045089.2:n.19A>C