Canonical Allele Identifier: CA1125097846
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825641248
gnomAD v3: 9-68578463-T-G
gnomAD v4: 9-68578463-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578463T>G , CM000671.2:g.68578463T>G GRCh38
NC_000009.11:g.71193379T>G , CM000671.1:g.71193379T>G GRCh37
NC_000009.10:g.70383199T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35821T>G
XR_001746701.2:n.342+35821T>G