Canonical Allele Identifier: CA588310932
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1482898441
gnomAD v2: 9-71193178-G-C
gnomAD v3: 9-68578262-G-C
gnomAD v4: 9-68578262-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578262G>C , CM000671.2:g.68578262G>C GRCh38
NC_000009.11:g.71193178G>C , CM000671.1:g.71193178G>C GRCh37
NC_000009.10:g.70382998G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35620G>C
XR_001746701.2:n.342+35620G>C