Canonical Allele Identifier: CA2613835801
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392277-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392277T>A , CM000673.2:g.61392277T>A GRCh38
NC_000011.9:g.61159749T>A , CM000673.1:g.61159749T>A GRCh37
NC_000011.8:g.60916325T>A NCBI36
NG_032976.1:g.4918T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-355T>A ENSP00000440638.1:n.-355T>A
XM_005274039.3:c.-686T>A XP_005274096.1:n.-686T>A
XM_005274039.4:c.-686T>A XP_005274096.1:n.-686T>A
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