Canonical Allele Identifier: CA866233754
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1488417216

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578277G>C , CM000671.2:g.68578277G>C GRCh38
NC_000009.11:g.71193193G>C , CM000671.1:g.71193193G>C GRCh37
NC_000009.10:g.70383013G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35635G>C
XR_001746701.2:n.342+35635G>C