Canonical Allele Identifier: CA193944084
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs556952338
gnomAD v3: 9-68578398-A-C
gnomAD v4: 9-68578398-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578398A>C , CM000671.2:g.68578398A>C GRCh38
NC_000009.11:g.71193314A>C , CM000671.1:g.71193314A>C GRCh37
NC_000009.10:g.70383134A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35756A>C
XR_001746701.2:n.342+35756A>C