Canonical Allele Identifier: CA193944078
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs926142994
gnomAD v3: 9-68578332-C-T
gnomAD v4: 9-68578332-C-T
MyVariant Identifiers: chr9:g.71193248C>T (hg19) chr9:g.68578332C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578332C>T , CM000671.2:g.68578332C>T GRCh38
NC_000009.11:g.71193248C>T , CM000671.1:g.71193248C>T GRCh37
NC_000009.10:g.70383068C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35690C>T
XR_001746701.2:n.342+35690C>T
Search 100 bp 5'
Search 100 bp 3'