Canonical Allele Identifier: CA561871816
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1419724780
gnomAD v2: 5-110413720-T-A
gnomAD v3: 5-111078022-T-A
gnomAD v4: 5-111078022-T-A
MyVariant Identifiers: chr5:g.110413720T>A (hg19) chr5:g.111078022T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111078022T>A , CM000667.2:g.111078022T>A GRCh38
NC_000005.9:g.110413720T>A , CM000667.1:g.110413720T>A GRCh37
NC_000005.8:g.110441619T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1948T>A MANE Select ENSP00000339804.3:n.*1948T>A
ENST00000379706.4:c.*1948T>A ENSP00000427827.1:n.*1948T>A
NM_033035.4:c.*1948T>A NP_149024.1:n.*1948T>A
NM_138551.4:c.*1948T>A NP_612561.2:n.*1948T>A
NR_045089.1:n.3832T>A
NM_033035.5:c.*1948T>A MANE Select NP_149024.1:n.*1948T>A
NM_138551.5:c.*1948T>A NP_612561.2:n.*1948T>A
NR_045089.2:n.3850T>A
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