Canonical Allele Identifier: CA222894227
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs898979819
MyVariant Identifiers: chr11:g.61159982G>C (hg19) chr11:g.61392510G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392510G>C , CM000673.2:g.61392510G>C GRCh38
NC_000011.9:g.61159982G>C , CM000673.1:g.61159982G>C GRCh37
NC_000011.8:g.60916558G>C NCBI36
NG_032976.1:g.5151G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-122G>C ENSP00000334844.5:n.-122G>C
ENST00000398979.7:c.-319G>C ENSP00000381950.3:n.-319G>C
ENST00000515837.6:c.-122G>C ENSP00000440638.1:n.-122G>C
NM_001173990.2:c.-122G>C NP_001167461.1:n.-122G>C
NM_001173991.2:c.-122G>C NP_001167462.1:n.-122G>C
NM_016499.5:c.-319G>C NP_057583.2:n.-319G>C
XM_005274039.3:c.-453G>C XP_005274096.1:n.-453G>C
NM_001330285.1:c.-319G>C NP_001317214.1:n.-319G>C
XM_005274039.4:c.-453G>C XP_005274096.1:n.-453G>C
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