Canonical Allele Identifier: CA445725842
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407603C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071905C>T , CM000667.2:g.111071905C>T GRCh38
NC_000005.9:g.110407603C>T , CM000667.1:g.110407603C>T GRCh37
NC_000005.8:g.110435502C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.15C>T MANE Select ENSP00000339804.3:p.Ala5=
ENST00000344895.3:c.15C>T ENSP00000339804.3:p.Ala5=
ENST00000420978.6:c.35-20C>T ENSP00000399099.2:n.35-20C>T
NM_033035.4:c.15C>T NP_149024.1:p.Ala5=
NR_045089.1:n.1439-20C>T
NM_033035.5:c.15C>T MANE Select NP_149024.1:p.Ala5=
NR_045089.2:n.1457-20C>T