Canonical Allele Identifier: CA2792320001
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392332T>C , CM000673.2:g.61392332T>C GRCh38
NC_000011.9:g.61159804T>C , CM000673.1:g.61159804T>C GRCh37
NC_000011.8:g.60916380T>C NCBI36
NG_032976.1:g.4973T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-300T>C ENSP00000440638.1:n.-300T>C
XM_005274039.3:c.-631T>C XP_005274096.1:n.-631T>C
XM_005274039.4:c.-631T>C XP_005274096.1:n.-631T>C