Canonical Allele Identifier: CA124873051

Gene: TSLP

Linked Data

• dbSNP Id: rs570910054
• gnomAD v3: 5-111071623-G-C
• gnomAD v4: 5-111071623-G-C
• MyVariant Identifiers: chr5:g.110407321G>C (hg19) ; chr5:g.111071623G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111071623G>C , CM000667.2:g.111071623G>C	GRCh38
NC_000005.9:g.110407321G>C , CM000667.1:g.110407321G>C	GRCh37
NC_000005.8:g.110435220G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420978.6:c.34+106G>C	ENSP00000399099.2:n.34+106G>C
NR_045089.1:n.1438+106G>C
NR_045089.2:n.1456+106G>C