Canonical Allele Identifier: CA445725884
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407660G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071962G>C , CM000667.2:g.111071962G>C GRCh38
NC_000005.9:g.110407660G>C , CM000667.1:g.110407660G>C GRCh37
NC_000005.8:g.110435559G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.72G>C MANE Select ENSP00000339804.3:p.Gly24=
ENST00000344895.3:c.72G>C ENSP00000339804.3:p.Gly24=
ENST00000420978.6:c.72G>C ENSP00000399099.2:p.Gly24=
NM_033035.4:c.72G>C NP_149024.1:p.Gly24=
NR_045089.1:n.1476G>C
NM_033035.5:c.72G>C MANE Select NP_149024.1:p.Gly24=
NR_045089.2:n.1494G>C
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