Canonical Allele Identifier: CA1125097746
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825638517
gnomAD v3: 9-68578168-C-A
gnomAD v4: 9-68578168-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578168C>A , CM000671.2:g.68578168C>A GRCh38
NC_000009.11:g.71193084C>A , CM000671.1:g.71193084C>A GRCh37
NC_000009.10:g.70382904C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35526C>A
XR_001746701.2:n.342+35526C>A