Canonical Allele Identifier: CA124873252
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1037586329
gnomAD v2: 5-110407531-T-C
gnomAD v3: 5-111071833-T-C
gnomAD v4: 5-111071833-T-C
MyVariant Identifiers: chr5:g.110407531T>C (hg19) chr5:g.111071833T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071833T>C , CM000667.2:g.111071833T>C GRCh38
NC_000005.9:g.110407531T>C , CM000667.1:g.110407531T>C GRCh37
NC_000005.8:g.110435430T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-58T>C MANE Select ENSP00000339804.3:n.-58T>C
ENST00000344895.3:c.-58T>C ENSP00000339804.3:n.-58T>C
ENST00000420978.6:c.35-92T>C ENSP00000399099.2:n.35-92T>C
NM_033035.4:c.-58T>C NP_149024.1:n.-58T>C
NR_045089.1:n.1439-92T>C
NM_033035.5:c.-58T>C MANE Select NP_149024.1:n.-58T>C
NR_045089.2:n.1457-92T>C
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