Canonical Allele Identifier: CA124874147
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs542008102
gnomAD v2: 5-110408102-A-C
gnomAD v3: 5-111072404-A-C
gnomAD v4: 5-111072404-A-C
MyVariant Identifiers: chr5:g.110408102A>C (hg19) chr5:g.111072404A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072404A>C , CM000667.2:g.111072404A>C GRCh38
NC_000005.9:g.110408102A>C , CM000667.1:g.110408102A>C GRCh37
NC_000005.8:g.110436001A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+343A>C MANE Select ENSP00000339804.3:n.171+343A>C
ENST00000344895.3:c.171+343A>C ENSP00000339804.3:n.171+343A>C
ENST00000420978.6:c.171+343A>C ENSP00000399099.2:n.171+343A>C
NM_033035.4:c.171+343A>C NP_149024.1:n.171+343A>C
NR_045089.1:n.1575+343A>C
NM_033035.5:c.171+343A>C MANE Select NP_149024.1:n.171+343A>C
NR_045089.2:n.1593+343A>C
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