Canonical Allele Identifier: CA1977295361
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392295A= , CM000673.2:g.61392295A= GRCh38
NC_000011.9:g.61159767A= , CM000673.1:g.61159767A= GRCh37
NC_000011.8:g.60916343A= NCBI36
NG_032976.1:g.4936A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-337A= ENSP00000440638.1:n.-337A=
XM_005274039.3:c.-668A= XP_005274096.1:n.-668A=
XM_005274039.4:c.-668A= XP_005274096.1:n.-668A=