Canonical Allele Identifier: CA866233810

Gene: TMEM252-DT

Linked Data

• dbSNP Id: rs913017582
• MyVariant Identifiers: chr9:g.71193321A>C (hg19) ; chr9:g.68578405A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.68578405A>C , CM000671.2:g.68578405A>C	GRCh38
NC_000009.11:g.71193321A>C , CM000671.1:g.71193321A>C	GRCh37
NC_000009.10:g.70383141A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929903.1:n.449+35763A>C
XR_001746701.2:n.342+35763A>C