Canonical Allele Identifier: CA2709815008
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs2112542071
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072238G>C , CM000667.2:g.111072238G>C GRCh38
NC_000005.9:g.110407936G>C , CM000667.1:g.110407936G>C GRCh37
NC_000005.8:g.110435835G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.171+177G>C MANE Select ENSP00000339804.3:n.171+177G>C
ENST00000344895.3:c.171+177G>C ENSP00000339804.3:n.171+177G>C
ENST00000420978.6:c.171+177G>C ENSP00000399099.2:n.171+177G>C
NM_033035.4:c.171+177G>C NP_149024.1:n.171+177G>C
NR_045089.1:n.1575+177G>C
NM_033035.5:c.171+177G>C MANE Select NP_149024.1:n.171+177G>C
NR_045089.2:n.1593+177G>C
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