Canonical Allele Identifier: CA2674827893
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v4: 5-111072122-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072122A>C , CM000667.2:g.111072122A>C GRCh38
NC_000005.9:g.110407820A>C , CM000667.1:g.110407820A>C GRCh37
NC_000005.8:g.110435719A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+61A>C MANE Select ENSP00000339804.3:n.171+61A>C
ENST00000344895.3:c.171+61A>C ENSP00000339804.3:n.171+61A>C
ENST00000420978.6:c.171+61A>C ENSP00000399099.2:n.171+61A>C
NM_033035.4:c.171+61A>C NP_149024.1:n.171+61A>C
NR_045089.1:n.1575+61A>C
NM_033035.5:c.171+61A>C MANE Select NP_149024.1:n.171+61A>C
NR_045089.2:n.1593+61A>C
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