Canonical Allele Identifier: CA1977295432
Gene: TMEM216 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392365C= , CM000673.2:g.61392365C= GRCh38
NC_000011.9:g.61159837C= , CM000673.1:g.61159837C= GRCh37
NC_000011.8:g.60916413C= NCBI36
NG_032976.1:g.5006C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-267C= ENSP00000334844.5:n.-267C=
ENST00000515837.6:c.-267C= ENSP00000440638.1:n.-267C=
NM_001173990.2:c.-267C= NP_001167461.1:n.-267C=
NM_001173991.2:c.-267C= NP_001167462.1:n.-267C=
XM_005274039.3:c.-598C= XP_005274096.1:n.-598C=
NM_001330285.1:c.-464C= NP_001317214.1:n.-464C=
XM_005274039.4:c.-598C= XP_005274096.1:n.-598C=
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