Canonical Allele Identifier: CA1977295358

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858688768

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392294G>C , CM000673.2:g.61392294G>C	GRCh38
NC_000011.9:g.61159766G>C , CM000673.1:g.61159766G>C	GRCh37
NC_000011.8:g.60916342G>C	NCBI36
NG_032976.1:g.4935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-338G>C	ENSP00000440638.1:n.-338G>C
XM_005274039.3:c.-669G>C	XP_005274096.1:n.-669G>C
XM_005274039.4:c.-669G>C	XP_005274096.1:n.-669G>C