Canonical Allele Identifier: CA2613835833
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392312-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392312G>A , CM000673.2:g.61392312G>A GRCh38
NC_000011.9:g.61159784G>A , CM000673.1:g.61159784G>A GRCh37
NC_000011.8:g.60916360G>A NCBI36
NG_032976.1:g.4953G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-320G>A ENSP00000440638.1:n.-320G>A
XM_005274039.3:c.-651G>A XP_005274096.1:n.-651G>A
XM_005274039.4:c.-651G>A XP_005274096.1:n.-651G>A
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