Canonical Allele Identifier: CA561869543
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1267246126
gnomAD v2: 5-110407246-G-A
gnomAD v4: 5-111071548-G-A
MyVariant Identifiers: chr5:g.110407246G>A (hg19) chr5:g.111071548G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071548G>A , CM000667.2:g.111071548G>A GRCh38
NC_000005.9:g.110407246G>A , CM000667.1:g.110407246G>A GRCh37
NC_000005.8:g.110435145G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+31G>A ENSP00000399099.2:n.34+31G>A
NR_045089.1:n.1438+31G>A
NR_045089.2:n.1456+31G>A
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