Canonical Allele Identifier: CA1977295565
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1236620234
gnomAD v4: 11-61392506-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392506G>A , CM000673.2:g.61392506G>A GRCh38
NC_000011.9:g.61159978G>A , CM000673.1:g.61159978G>A GRCh37
NC_000011.8:g.60916554G>A NCBI36
NG_032976.1:g.5147G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-126G>A ENSP00000334844.5:n.-126G>A
ENST00000398979.7:c.-323G>A ENSP00000381950.3:n.-323G>A
ENST00000515837.6:c.-126G>A ENSP00000440638.1:n.-126G>A
NM_001173990.2:c.-126G>A NP_001167461.1:n.-126G>A
NM_001173991.2:c.-126G>A NP_001167462.1:n.-126G>A
NM_016499.5:c.-323G>A NP_057583.2:n.-323G>A
XM_005274039.3:c.-457G>A XP_005274096.1:n.-457G>A
NM_001330285.1:c.-323G>A NP_001317214.1:n.-323G>A
XM_005274039.4:c.-457G>A XP_005274096.1:n.-457G>A
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