Canonical Allele Identifier: CA1125097779
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825639941
gnomAD v3: 9-68578279-G-T
gnomAD v4: 9-68578279-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578279G>T , CM000671.2:g.68578279G>T GRCh38
NC_000009.11:g.71193195G>T , CM000671.1:g.71193195G>T GRCh37
NC_000009.10:g.70383015G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35637G>T
XR_001746701.2:n.342+35637G>T