Canonical Allele Identifier: CA1977295340
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392268G= , CM000673.2:g.61392268G= GRCh38
NC_000011.9:g.61159740G= , CM000673.1:g.61159740G= GRCh37
NC_000011.8:g.60916316G= NCBI36
NG_032976.1:g.4909G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-364G= ENSP00000440638.1:n.-364G=
XM_005274039.3:c.-695G= XP_005274096.1:n.-695G=
XM_005274039.4:c.-695G= XP_005274096.1:n.-695G=