Canonical Allele Identifier: CA866233798
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1303982228
gnomAD v3: 9-68578386-A-G
gnomAD v4: 9-68578386-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578386A>G , CM000671.2:g.68578386A>G GRCh38
NC_000009.11:g.71193302A>G , CM000671.1:g.71193302A>G GRCh37
NC_000009.10:g.70383122A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35744A>G
XR_001746701.2:n.342+35744A>G