Canonical Allele Identifier: CA801887593
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1362508549
MyVariant Identifiers: chr5:g.110408063G>A (hg19) chr5:g.111072365G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072365G>A , CM000667.2:g.111072365G>A GRCh38
NC_000005.9:g.110408063G>A , CM000667.1:g.110408063G>A GRCh37
NC_000005.8:g.110435962G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+304G>A MANE Select ENSP00000339804.3:n.171+304G>A
ENST00000344895.3:c.171+304G>A ENSP00000339804.3:n.171+304G>A
ENST00000420978.6:c.171+304G>A ENSP00000399099.2:n.171+304G>A
NM_033035.4:c.171+304G>A NP_149024.1:n.171+304G>A
NR_045089.1:n.1575+304G>A
NM_033035.5:c.171+304G>A MANE Select NP_149024.1:n.171+304G>A
NR_045089.2:n.1593+304G>A
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