Canonical Allele Identifier: CA360602328
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407200A>C (hg19) chr5:g.111071502A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071502A>C , CM000667.2:g.111071502A>C GRCh38
NC_000005.9:g.110407200A>C , CM000667.1:g.110407200A>C GRCh37
NC_000005.8:g.110435099A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.19A>C ENSP00000399099.2:p.Ser7Arg
NR_045089.1:n.1423A>C
NR_045089.2:n.1441A>C
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