Canonical Allele Identifier: CA2613835878
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392360-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392360A>T , CM000673.2:g.61392360A>T GRCh38
NC_000011.9:g.61159832A>T , CM000673.1:g.61159832A>T GRCh37
NC_000011.8:g.60916408A>T NCBI36
NG_032976.1:g.5001A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-272A>T ENSP00000334844.5:n.-272A>T
ENST00000515837.6:c.-272A>T ENSP00000440638.1:n.-272A>T
NM_001173990.2:c.-272A>T NP_001167461.1:n.-272A>T
NM_001173991.2:c.-272A>T NP_001167462.1:n.-272A>T
XM_005274039.3:c.-603A>T XP_005274096.1:n.-603A>T
NM_001330285.1:c.-469A>T NP_001317214.1:n.-469A>T
XM_005274039.4:c.-603A>T XP_005274096.1:n.-603A>T
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