Canonical Allele Identifier: CA2792319999
Gene: TMEM216 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392327G>A , CM000673.2:g.61392327G>A GRCh38
NC_000011.9:g.61159799G>A , CM000673.1:g.61159799G>A GRCh37
NC_000011.8:g.60916375G>A NCBI36
NG_032976.1:g.4968G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-305G>A ENSP00000440638.1:n.-305G>A
XM_005274039.3:c.-636G>A XP_005274096.1:n.-636G>A
XM_005274039.4:c.-636G>A XP_005274096.1:n.-636G>A
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