Canonical Allele Identifier: CA2613835817
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs2135188539
gnomAD v4: 11-61392293-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392293T>A , CM000673.2:g.61392293T>A GRCh38
NC_000011.9:g.61159765T>A , CM000673.1:g.61159765T>A GRCh37
NC_000011.8:g.60916341T>A NCBI36
NG_032976.1:g.4934T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-339T>A ENSP00000440638.1:n.-339T>A
XM_005274039.3:c.-670T>A XP_005274096.1:n.-670T>A
XM_005274039.4:c.-670T>A XP_005274096.1:n.-670T>A
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