Canonical Allele Identifier: CA1977295390
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392334T= , CM000673.2:g.61392334T= GRCh38
NC_000011.9:g.61159806T= , CM000673.1:g.61159806T= GRCh37
NC_000011.8:g.60916382T= NCBI36
NG_032976.1:g.4975T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-298T= ENSP00000440638.1:n.-298T=
XM_005274039.3:c.-629T= XP_005274096.1:n.-629T=
XM_005274039.4:c.-629T= XP_005274096.1:n.-629T=