Canonical Allele Identifier: CA801857041
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1450518104
MyVariant Identifiers: chr5:g.110413598T>A (hg19) chr5:g.111077900T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077900T>A , CM000667.2:g.111077900T>A GRCh38
NC_000005.9:g.110413598T>A , CM000667.1:g.110413598T>A GRCh37
NC_000005.8:g.110441497T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*1826T>A MANE Select ENSP00000339804.3:n.*1826T>A
ENST00000379706.4:c.*1826T>A ENSP00000427827.1:n.*1826T>A
NM_033035.4:c.*1826T>A NP_149024.1:n.*1826T>A
NM_138551.4:c.*1826T>A NP_612561.2:n.*1826T>A
NR_045089.1:n.3710T>A
NM_033035.5:c.*1826T>A MANE Select NP_149024.1:n.*1826T>A
NM_138551.5:c.*1826T>A NP_612561.2:n.*1826T>A
NR_045089.2:n.3728T>A
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