Canonical Allele Identifier: CA360602429
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407613G>T (hg19) chr5:g.111071915G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071915G>T , CM000667.2:g.111071915G>T GRCh38
NC_000005.9:g.110407613G>T , CM000667.1:g.110407613G>T GRCh37
NC_000005.8:g.110435512G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.25G>T MANE Select ENSP00000339804.3:p.Val9Phe
ENST00000344895.3:c.25G>T ENSP00000339804.3:p.Val9Phe
ENST00000420978.6:c.35-10G>T ENSP00000399099.2:n.35-10G>T
NM_033035.4:c.25G>T NP_149024.1:p.Val9Phe
NR_045089.1:n.1439-10G>T
NM_033035.5:c.25G>T MANE Select NP_149024.1:p.Val9Phe
NR_045089.2:n.1457-10G>T
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