Canonical Allele Identifier: CA193944060
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1003328416

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578207T>C , CM000671.2:g.68578207T>C GRCh38
NC_000009.11:g.71193123T>C , CM000671.1:g.71193123T>C GRCh37
NC_000009.10:g.70382943T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929903.1:n.449+35565T>C
XR_001746701.2:n.342+35565T>C