Canonical Allele Identifier: CA1977295354
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392292T= , CM000673.2:g.61392292T= GRCh38
NC_000011.9:g.61159764T= , CM000673.1:g.61159764T= GRCh37
NC_000011.8:g.60916340T= NCBI36
NG_032976.1:g.4933T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-340T= ENSP00000440638.1:n.-340T=
XM_005274039.3:c.-671T= XP_005274096.1:n.-671T=
XM_005274039.4:c.-671T= XP_005274096.1:n.-671T=