Canonical Allele Identifier: CA801856638
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1356470169
gnomAD v3: 5-111077122-G-A
gnomAD v4: 5-111077122-G-A
MyVariant Identifiers: chr5:g.110412820G>A (hg19) chr5:g.111077122G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111077122G>A , CM000667.2:g.111077122G>A GRCh38
NC_000005.9:g.110412820G>A , CM000667.1:g.110412820G>A GRCh37
NC_000005.8:g.110440719G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.*1048G>A MANE Select ENSP00000339804.3:n.*1048G>A
ENST00000379706.4:c.*1048G>A ENSP00000427827.1:n.*1048G>A
NM_033035.4:c.*1048G>A NP_149024.1:n.*1048G>A
NM_138551.4:c.*1048G>A NP_612561.2:n.*1048G>A
NR_045089.1:n.2932G>A
NM_033035.5:c.*1048G>A MANE Select NP_149024.1:n.*1048G>A
NM_138551.5:c.*1048G>A NP_612561.2:n.*1048G>A
NR_045089.2:n.2950G>A
Search 100 bp 5'
Search 100 bp 3'