Canonical Allele Identifier: CA562217225
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1246762679
gnomAD v2: 5-110407465-G-C
gnomAD v3: 5-111071767-G-C
gnomAD v4: 5-111071767-G-C
MyVariant Identifiers: chr5:g.110407465G>C (hg19) chr5:g.111071767G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071767G>C , CM000667.2:g.111071767G>C GRCh38
NC_000005.9:g.110407465G>C , CM000667.1:g.110407465G>C GRCh37
NC_000005.8:g.110435364G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-124G>C MANE Select ENSP00000339804.3:n.-124G>C
ENST00000344895.3:c.-124G>C ENSP00000339804.3:n.-124G>C
ENST00000420978.6:c.35-158G>C ENSP00000399099.2:n.35-158G>C
NM_033035.4:c.-124G>C NP_149024.1:n.-124G>C
NR_045089.1:n.1439-158G>C
NM_033035.5:c.-124G>C MANE Select NP_149024.1:n.-124G>C
NR_045089.2:n.1457-158G>C
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