Canonical Allele Identifier: CA2792319994
Gene: TMEM216 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392316A>T , CM000673.2:g.61392316A>T GRCh38
NC_000011.9:g.61159788A>T , CM000673.1:g.61159788A>T GRCh37
NC_000011.8:g.60916364A>T NCBI36
NG_032976.1:g.4957A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-316A>T ENSP00000440638.1:n.-316A>T
XM_005274039.3:c.-647A>T XP_005274096.1:n.-647A>T
XM_005274039.4:c.-647A>T XP_005274096.1:n.-647A>T
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