Canonical Allele Identifier: CA1977295398
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392337T= , CM000673.2:g.61392337T= GRCh38
NC_000011.9:g.61159809T= , CM000673.1:g.61159809T= GRCh37
NC_000011.8:g.60916385T= NCBI36
NG_032976.1:g.4978T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-295T= ENSP00000440638.1:n.-295T=
XM_005274039.3:c.-626T= XP_005274096.1:n.-626T=
XM_005274039.4:c.-626T= XP_005274096.1:n.-626T=