Canonical Allele Identifier: CA193944075
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs974995019

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578325T>C , CM000671.2:g.68578325T>C GRCh38
NC_000009.11:g.71193241T>C , CM000671.1:g.71193241T>C GRCh37
NC_000009.10:g.70383061T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35683T>C
XR_001746701.2:n.342+35683T>C