Canonical Allele Identifier: CA2613835883
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392369C>A , CM000673.2:g.61392369C>A GRCh38
NC_000011.9:g.61159841C>A , CM000673.1:g.61159841C>A GRCh37
NC_000011.8:g.60916417C>A NCBI36
NG_032976.1:g.5010C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-263C>A ENSP00000334844.5:n.-263C>A
ENST00000515837.6:c.-263C>A ENSP00000440638.1:n.-263C>A
NM_001173990.2:c.-263C>A NP_001167461.1:n.-263C>A
NM_001173991.2:c.-263C>A NP_001167462.1:n.-263C>A
XM_005274039.3:c.-594C>A XP_005274096.1:n.-594C>A
NM_001330285.1:c.-460C>A NP_001317214.1:n.-460C>A
XM_005274039.4:c.-594C>A XP_005274096.1:n.-594C>A