Canonical Allele Identifier: CA360602522
Gene: TSLP HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.111071960G>C
GRCh37 chr5:g.110407658G>C
Revel Score:
ENST00000420978 0.069
ENST00000344895 (MANE Select) 0.069
ClinVar RCV:
RCV004172194
ClinVar Variation:
2329524
dbSNP:
1179899313
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071960G>C , CM000667.2:g.111071960G>C GRCh38
NC_000005.9:g.110407658G>C , CM000667.1:g.110407658G>C GRCh37
NC_000005.8:g.110435557G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.70G>C MANE Select ENSP00000339804.3:p.Gly24Arg
ENST00000344895.3:c.70G>C ENSP00000339804.3:p.Gly24Arg
ENST00000420978.6:c.70G>C ENSP00000399099.2:p.Gly24Arg
NM_033035.4:c.70G>C NP_149024.1:p.Gly24Arg
NR_045089.1:n.1474G>C
NM_033035.5:c.70G>C MANE Select NP_149024.1:p.Gly24Arg
NR_045089.2:n.1492G>C
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