Canonical Allele Identifier: CA1853838248
Gene: TMEM252-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578331A= , CM000671.2:g.68578331A= GRCh38
NC_000009.11:g.71193247A= , CM000671.1:g.71193247A= GRCh37
NC_000009.10:g.70383067A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35689A=
XR_001746701.2:n.342+35689A=