Canonical Allele Identifier: CA2613835861
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392338-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392338G>T , CM000673.2:g.61392338G>T GRCh38
NC_000011.9:g.61159810G>T , CM000673.1:g.61159810G>T GRCh37
NC_000011.8:g.60916386G>T NCBI36
NG_032976.1:g.4979G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-294G>T ENSP00000440638.1:n.-294G>T
XM_005274039.3:c.-625G>T XP_005274096.1:n.-625G>T
XM_005274039.4:c.-625G>T XP_005274096.1:n.-625G>T
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