Canonical Allele Identifier: CA866233706
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1214591682
gnomAD v3: 9-68578199-A-T
gnomAD v4: 9-68578199-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578199A>T , CM000671.2:g.68578199A>T GRCh38
NC_000009.11:g.71193115A>T , CM000671.1:g.71193115A>T GRCh37
NC_000009.10:g.70382935A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929903.1:n.449+35557A>T
XR_001746701.2:n.342+35557A>T