Canonical Allele Identifier: CA1977295357
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392294G= , CM000673.2:g.61392294G= GRCh38
NC_000011.9:g.61159766G= , CM000673.1:g.61159766G= GRCh37
NC_000011.8:g.60916342G= NCBI36
NG_032976.1:g.4935G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-338G= ENSP00000440638.1:n.-338G=
XM_005274039.3:c.-669G= XP_005274096.1:n.-669G=
XM_005274039.4:c.-669G= XP_005274096.1:n.-669G=