Canonical Allele Identifier: CA678971509
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs942984864
gnomAD v4: 11-61392268-G-C
MyVariant Identifiers: chr11:g.61159740G>C (hg19) chr11:g.61392268G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392268G>C , CM000673.2:g.61392268G>C GRCh38
NC_000011.9:g.61159740G>C , CM000673.1:g.61159740G>C GRCh37
NC_000011.8:g.60916316G>C NCBI36
NG_032976.1:g.4909G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-364G>C ENSP00000440638.1:n.-364G>C
XM_005274039.3:c.-695G>C XP_005274096.1:n.-695G>C
XM_005274039.4:c.-695G>C XP_005274096.1:n.-695G>C
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