Canonical Allele Identifier: CA599502936
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1445600918
gnomAD v2: 11-61159759-T-C
gnomAD v3: 11-61392287-T-C
gnomAD v4: 11-61392287-T-C
MyVariant Identifiers: chr11:g.61159759T>C (hg19) chr11:g.61392287T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392287T>C , CM000673.2:g.61392287T>C GRCh38
NC_000011.9:g.61159759T>C , CM000673.1:g.61159759T>C GRCh37
NC_000011.8:g.60916335T>C NCBI36
NG_032976.1:g.4928T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-345T>C ENSP00000440638.1:n.-345T>C
XM_005274039.3:c.-676T>C XP_005274096.1:n.-676T>C
XM_005274039.4:c.-676T>C XP_005274096.1:n.-676T>C
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