Canonical Allele Identifier: CA562217226

Gene: TSLP

Linked Data

• dbSNP Id: rs1468459767
• gnomAD v2: 5-110407475-G-A
• gnomAD v3: 5-111071777-G-A
• gnomAD v4: 5-111071777-G-A
• MyVariant Identifiers: chr5:g.110407475G>A (hg19) ; chr5:g.111071777G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111071777G>A , CM000667.2:g.111071777G>A	GRCh38
NC_000005.9:g.110407475G>A , CM000667.1:g.110407475G>A	GRCh37
NC_000005.8:g.110435374G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.-114G>A MANE Select	ENSP00000339804.3:n.-114G>A
ENST00000344895.3:c.-114G>A	ENSP00000339804.3:n.-114G>A
ENST00000420978.6:c.35-148G>A	ENSP00000399099.2:n.35-148G>A
NM_033035.4:c.-114G>A	NP_149024.1:n.-114G>A
NR_045089.1:n.1439-148G>A
NM_033035.5:c.-114G>A MANE Select	NP_149024.1:n.-114G>A
NR_045089.2:n.1457-148G>A