Canonical Allele Identifier: CA2613835818
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392293-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392293T>C , CM000673.2:g.61392293T>C GRCh38
NC_000011.9:g.61159765T>C , CM000673.1:g.61159765T>C GRCh37
NC_000011.8:g.60916341T>C NCBI36
NG_032976.1:g.4934T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-339T>C ENSP00000440638.1:n.-339T>C
XM_005274039.3:c.-670T>C XP_005274096.1:n.-670T>C
XM_005274039.4:c.-670T>C XP_005274096.1:n.-670T>C
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