Canonical Allele Identifier: CA2613835876
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392358-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392358C>T , CM000673.2:g.61392358C>T GRCh38
NC_000011.9:g.61159830C>T , CM000673.1:g.61159830C>T GRCh37
NC_000011.8:g.60916406C>T NCBI36
NG_032976.1:g.4999C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-274C>T ENSP00000440638.1:n.-274C>T
XM_005274039.3:c.-605C>T XP_005274096.1:n.-605C>T
XM_005274039.4:c.-605C>T XP_005274096.1:n.-605C>T
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