Canonical Allele Identifier: CA599502934
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1331332167
gnomAD v2: 11-61159748-C-T
gnomAD v3: 11-61392276-C-T
gnomAD v4: 11-61392276-C-T
MyVariant Identifiers: chr11:g.61159748C>T (hg19) chr11:g.61392276C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392276C>T , CM000673.2:g.61392276C>T GRCh38
NC_000011.9:g.61159748C>T , CM000673.1:g.61159748C>T GRCh37
NC_000011.8:g.60916324C>T NCBI36
NG_032976.1:g.4917C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-356C>T ENSP00000440638.1:n.-356C>T
XM_005274039.3:c.-687C>T XP_005274096.1:n.-687C>T
XM_005274039.4:c.-687C>T XP_005274096.1:n.-687C>T
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