Canonical Allele Identifier: CA360602548

Gene: TSLP

Linked Data

• MyVariant Identifiers: chr5:g.110407671C>G (hg19) ; chr5:g.111071973C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111071973C>G , CM000667.2:g.111071973C>G	GRCh38
NC_000005.9:g.110407671C>G , CM000667.1:g.110407671C>G	GRCh37
NC_000005.8:g.110435570C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344895.4:c.83C>G MANE Select	ENSP00000339804.3:p.Thr28Ser
ENST00000344895.3:c.83C>G	ENSP00000339804.3:p.Thr28Ser
ENST00000420978.6:c.83C>G	ENSP00000399099.2:p.Thr28Ser
NM_033035.4:c.83C>G	NP_149024.1:p.Thr28Ser
NR_045089.1:n.1487C>G
NM_033035.5:c.83C>G MANE Select	NP_149024.1:p.Thr28Ser
NR_045089.2:n.1505C>G