Canonical Allele Identifier: CA1853838250
Gene: TMEM252-DT HGNC NCBI

Linked Data

dbSNP Id: rs926142994

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578332C>A , CM000671.2:g.68578332C>A GRCh38
NC_000009.11:g.71193248C>A , CM000671.1:g.71193248C>A GRCh37
NC_000009.10:g.70383068C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35690C>A
XR_001746701.2:n.342+35690C>A