Canonical Allele Identifier: CA561869630

Gene: TSLP

Linked Data

• dbSNP Id: rs1280033289
• gnomAD v2: 5-110408061-A-C
• gnomAD v3: 5-111072363-A-C
• gnomAD v4: 5-111072363-A-C
• MyVariant Identifiers: chr5:g.110408061A>C (hg19) ; chr5:g.111072363A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111072363A>C , CM000667.2:g.111072363A>C	GRCh38
NC_000005.9:g.110408061A>C , CM000667.1:g.110408061A>C	GRCh37
NC_000005.8:g.110435960A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.171+302A>C MANE Select	ENSP00000339804.3:n.171+302A>C
ENST00000344895.3:c.171+302A>C	ENSP00000339804.3:n.171+302A>C
ENST00000420978.6:c.171+302A>C	ENSP00000399099.2:n.171+302A>C
NM_033035.4:c.171+302A>C	NP_149024.1:n.171+302A>C
NR_045089.1:n.1575+302A>C
NM_033035.5:c.171+302A>C MANE Select	NP_149024.1:n.171+302A>C
NR_045089.2:n.1593+302A>C