Canonical Allele Identifier: CA2613835900
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392382-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392382T>A , CM000673.2:g.61392382T>A GRCh38
NC_000011.9:g.61159854T>A , CM000673.1:g.61159854T>A GRCh37
NC_000011.8:g.60916430T>A NCBI36
NG_032976.1:g.5023T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-250T>A ENSP00000334844.5:n.-250T>A
ENST00000515837.6:c.-250T>A ENSP00000440638.1:n.-250T>A
NM_001173990.2:c.-250T>A NP_001167461.1:n.-250T>A
NM_001173991.2:c.-250T>A NP_001167462.1:n.-250T>A
XM_005274039.3:c.-581T>A XP_005274096.1:n.-581T>A
NM_001330285.1:c.-447T>A NP_001317214.1:n.-447T>A
XM_005274039.4:c.-581T>A XP_005274096.1:n.-581T>A
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