Canonical Allele Identifier: CA360602352
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1412325631
gnomAD v2: 5-110407209-G-C
gnomAD v4: 5-111071511-G-C
MyVariant Identifiers: chr5:g.110407209G>C (hg19) chr5:g.111071511G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071511G>C , CM000667.2:g.111071511G>C GRCh38
NC_000005.9:g.110407209G>C , CM000667.1:g.110407209G>C GRCh37
NC_000005.8:g.110435108G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.28G>C ENSP00000399099.2:p.Glu10Gln
NR_045089.1:n.1432G>C
NR_045089.2:n.1450G>C
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