Canonical Allele Identifier: CA2792319992
Gene: TMEM216 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392310G>A , CM000673.2:g.61392310G>A GRCh38
NC_000011.9:g.61159782G>A , CM000673.1:g.61159782G>A GRCh37
NC_000011.8:g.60916358G>A NCBI36
NG_032976.1:g.4951G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-322G>A ENSP00000440638.1:n.-322G>A
XM_005274039.3:c.-653G>A XP_005274096.1:n.-653G>A
XM_005274039.4:c.-653G>A XP_005274096.1:n.-653G>A
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