Canonical Allele Identifier: CA678971511
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1198798344
gnomAD v3: 11-61392315-T-C
gnomAD v4: 11-61392315-T-C
MyVariant Identifiers: chr11:g.61159787T>C (hg19) chr11:g.61392315T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392315T>C , CM000673.2:g.61392315T>C GRCh38
NC_000011.9:g.61159787T>C , CM000673.1:g.61159787T>C GRCh37
NC_000011.8:g.60916363T>C NCBI36
NG_032976.1:g.4956T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-317T>C ENSP00000440638.1:n.-317T>C
XM_005274039.3:c.-648T>C XP_005274096.1:n.-648T>C
XM_005274039.4:c.-648T>C XP_005274096.1:n.-648T>C
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