Canonical Allele Identifier: CA678971517
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1046972319
gnomAD v4: 11-61392337-T-A
MyVariant Identifiers: chr11:g.61159809T>A (hg19) chr11:g.61392337T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392337T>A , CM000673.2:g.61392337T>A GRCh38
NC_000011.9:g.61159809T>A , CM000673.1:g.61159809T>A GRCh37
NC_000011.8:g.60916385T>A NCBI36
NG_032976.1:g.4978T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-295T>A ENSP00000440638.1:n.-295T>A
XM_005274039.3:c.-626T>A XP_005274096.1:n.-626T>A
XM_005274039.4:c.-626T>A XP_005274096.1:n.-626T>A
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