Canonical Allele Identifier: CA1853838229
Gene: TMEM252-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.68578261A= , CM000671.2:g.68578261A= GRCh38
NC_000009.11:g.71193177A= , CM000671.1:g.71193177A= GRCh37
NC_000009.10:g.70382997A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929903.1:n.449+35619A=
XR_001746701.2:n.342+35619A=