Canonical Allele Identifier: CA124874173
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1005856844
gnomAD v3: 5-111072442-C-G
gnomAD v4: 5-111072442-C-G
MyVariant Identifiers: chr5:g.111072442C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072442C>G , CM000667.2:g.111072442C>G GRCh38
NC_000005.9:g.110408140C>G , CM000667.1:g.110408140C>G GRCh37
NC_000005.8:g.110436039C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+381C>G MANE Select ENSP00000339804.3:n.171+381C>G
ENST00000344895.3:c.171+381C>G ENSP00000339804.3:n.171+381C>G
ENST00000420978.6:c.171+381C>G ENSP00000399099.2:n.171+381C>G
NM_033035.4:c.171+381C>G NP_149024.1:n.171+381C>G
NR_045089.1:n.1575+381C>G
NM_033035.5:c.171+381C>G MANE Select NP_149024.1:n.171+381C>G
NR_045089.2:n.1593+381C>G
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