Canonical Allele Identifier: CA445727868
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110412729G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077031G>C , CM000667.2:g.111077031G>C GRCh38
NC_000005.9:g.110412729G>C , CM000667.1:g.110412729G>C GRCh37
NC_000005.8:g.110440628G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.*957G>C MANE Select ENSP00000339804.3:n.*957G>C
ENST00000379706.4:c.*957G>C ENSP00000427827.1:n.*957G>C
NM_033035.4:c.*957G>C NP_149024.1:n.*957G>C
NM_138551.4:c.*957G>C NP_612561.2:n.*957G>C
NR_045089.1:n.2841G>C
NM_033035.5:c.*957G>C MANE Select NP_149024.1:n.*957G>C
NM_138551.5:c.*957G>C NP_612561.2:n.*957G>C
NR_045089.2:n.2859G>C
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