Canonical Allele Identifier: CA2613835798
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392273-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392273C>A , CM000673.2:g.61392273C>A GRCh38
NC_000011.9:g.61159745C>A , CM000673.1:g.61159745C>A GRCh37
NC_000011.8:g.60916321C>A NCBI36
NG_032976.1:g.4914C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-359C>A ENSP00000440638.1:n.-359C>A
XM_005274039.3:c.-690C>A XP_005274096.1:n.-690C>A
XM_005274039.4:c.-690C>A XP_005274096.1:n.-690C>A
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