Canonical Allele Identifier: CA445725832
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1427854002
gnomAD v3: 5-111071859-T-G
gnomAD v4: 5-111071859-T-G
MyVariant Identifiers: chr5:g.110407557T>G (hg19) chr5:g.111071859T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071859T>G , CM000667.2:g.111071859T>G GRCh38
NC_000005.9:g.110407557T>G , CM000667.1:g.110407557T>G GRCh37
NC_000005.8:g.110435456T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-32T>G MANE Select ENSP00000339804.3:n.-32T>G
ENST00000344895.3:c.-32T>G ENSP00000339804.3:n.-32T>G
ENST00000420978.6:c.35-66T>G ENSP00000399099.2:n.35-66T>G
NM_033035.4:c.-32T>G NP_149024.1:n.-32T>G
NR_045089.1:n.1439-66T>G
NM_033035.5:c.-32T>G MANE Select NP_149024.1:n.-32T>G
NR_045089.2:n.1457-66T>G
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