Canonical Allele Identifier: CA1853838285
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs1825640921

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578402C>T , CM000671.2:g.68578402C>T GRCh38
NC_000009.11:g.71193318C>T , CM000671.1:g.71193318C>T GRCh37
NC_000009.10:g.70383138C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35760C>T
XR_001746701.2:n.342+35760C>T