Canonical Allele Identifier: CA124873400

Gene: TSLP

Linked Data

• dbSNP Id: rs904269166
• gnomAD v2: 5-110407583-C-G
• gnomAD v3: 5-111071885-C-G
• gnomAD v4: 5-111071885-C-G
• MyVariant Identifiers: chr5:g.110407583C>G (hg19) ; chr5:g.111071885C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111071885C>G , CM000667.2:g.111071885C>G	GRCh38
NC_000005.9:g.110407583C>G , CM000667.1:g.110407583C>G	GRCh37
NC_000005.8:g.110435482C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.-6C>G MANE Select	ENSP00000339804.3:n.-6C>G
ENST00000344895.3:c.-6C>G	ENSP00000339804.3:n.-6C>G
ENST00000420978.6:c.35-40C>G	ENSP00000399099.2:n.35-40C>G
NM_033035.4:c.-6C>G	NP_149024.1:n.-6C>G
NR_045089.1:n.1439-40C>G
NM_033035.5:c.-6C>G MANE Select	NP_149024.1:n.-6C>G
NR_045089.2:n.1457-40C>G