Canonical Allele Identifier: CA1977295366

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858688926

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392306T>C , CM000673.2:g.61392306T>C	GRCh38
NC_000011.9:g.61159778T>C , CM000673.1:g.61159778T>C	GRCh37
NC_000011.8:g.60916354T>C	NCBI36
NG_032976.1:g.4947T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-326T>C	ENSP00000440638.1:n.-326T>C
XM_005274039.3:c.-657T>C	XP_005274096.1:n.-657T>C
XM_005274039.4:c.-657T>C	XP_005274096.1:n.-657T>C