Canonical Allele Identifier: CA193944072
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs965340162

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578272C>T , CM000671.2:g.68578272C>T GRCh38
NC_000009.11:g.71193188C>T , CM000671.1:g.71193188C>T GRCh37
NC_000009.10:g.70383008C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35630C>T
XR_001746701.2:n.342+35630C>T