Canonical Allele Identifier: CA1125097818
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825640597
gnomAD v3: 9-68578370-G-A
gnomAD v4: 9-68578370-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578370G>A , CM000671.2:g.68578370G>A GRCh38
NC_000009.11:g.71193286G>A , CM000671.1:g.71193286G>A GRCh37
NC_000009.10:g.70383106G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35728G>A
XR_001746701.2:n.342+35728G>A