Canonical Allele Identifier: CA2792319986
Gene: TMEM216 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392276C>A , CM000673.2:g.61392276C>A GRCh38
NC_000011.9:g.61159748C>A , CM000673.1:g.61159748C>A GRCh37
NC_000011.8:g.60916324C>A NCBI36
NG_032976.1:g.4917C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-356C>A ENSP00000440638.1:n.-356C>A
XM_005274039.3:c.-687C>A XP_005274096.1:n.-687C>A
XM_005274039.4:c.-687C>A XP_005274096.1:n.-687C>A
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