Canonical Allele Identifier: CA562217234
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1363708796
gnomAD v2: 5-110407569-G-T
gnomAD v4: 5-111071871-G-T
MyVariant Identifiers: chr5:g.110407569G>T (hg19) chr5:g.111071871G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071871G>T , CM000667.2:g.111071871G>T GRCh38
NC_000005.9:g.110407569G>T , CM000667.1:g.110407569G>T GRCh37
NC_000005.8:g.110435468G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-20G>T MANE Select ENSP00000339804.3:n.-20G>T
ENST00000344895.3:c.-20G>T ENSP00000339804.3:n.-20G>T
ENST00000420978.6:c.35-54G>T ENSP00000399099.2:n.35-54G>T
NM_033035.4:c.-20G>T NP_149024.1:n.-20G>T
NR_045089.1:n.1439-54G>T
NM_033035.5:c.-20G>T MANE Select NP_149024.1:n.-20G>T
NR_045089.2:n.1457-54G>T
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