Canonical Allele Identifier: CA2613835792
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392267-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392267C>T , CM000673.2:g.61392267C>T GRCh38
NC_000011.9:g.61159739C>T , CM000673.1:g.61159739C>T GRCh37
NC_000011.8:g.60916315C>T NCBI36
NG_032976.1:g.4908C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-365C>T ENSP00000440638.1:n.-365C>T
XM_005274039.3:c.-696C>T XP_005274096.1:n.-696C>T
XM_005274039.4:c.-696C>T XP_005274096.1:n.-696C>T
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