Canonical Allele Identifier: CA2709814674
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs2112541307
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071745G>C , CM000667.2:g.111071745G>C GRCh38
NC_000005.9:g.110407443G>C , CM000667.1:g.110407443G>C GRCh37
NC_000005.8:g.110435342G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-146G>C MANE Select ENSP00000339804.3:n.-146G>C
ENST00000344895.3:c.-146G>C ENSP00000339804.3:n.-146G>C
ENST00000420978.6:c.35-180G>C ENSP00000399099.2:n.35-180G>C
NM_033035.4:c.-146G>C NP_149024.1:n.-146G>C
NR_045089.1:n.1439-180G>C
NM_033035.5:c.-146G>C MANE Select NP_149024.1:n.-146G>C
NR_045089.2:n.1457-180G>C
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