Canonical Allele Identifier: CA193944082

Gene: TMEM252-DT

Linked Data

• dbSNP Id: rs537705907
• MyVariant Identifiers: chr9:g.71193307T>C (hg19) ; chr9:g.68578391T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.68578391T>C , CM000671.2:g.68578391T>C	GRCh38
NC_000009.11:g.71193307T>C , CM000671.1:g.71193307T>C	GRCh37
NC_000009.10:g.70383127T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929903.1:n.449+35749T>C
XR_001746701.2:n.342+35749T>C