Canonical Allele Identifier: CA678971523
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1441876653
gnomAD v4: 11-61392386-A-G
MyVariant Identifiers: chr11:g.61159858A>G (hg19) chr11:g.61392386A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392386A>G , CM000673.2:g.61392386A>G GRCh38
NC_000011.9:g.61159858A>G , CM000673.1:g.61159858A>G GRCh37
NC_000011.8:g.60916434A>G NCBI36
NG_032976.1:g.5027A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-246A>G ENSP00000334844.5:n.-246A>G
ENST00000515837.6:c.-246A>G ENSP00000440638.1:n.-246A>G
NM_001173990.2:c.-246A>G NP_001167461.1:n.-246A>G
NM_001173991.2:c.-246A>G NP_001167462.1:n.-246A>G
XM_005274039.3:c.-577A>G XP_005274096.1:n.-577A>G
NM_001330285.1:c.-443A>G NP_001317214.1:n.-443A>G
XM_005274039.4:c.-577A>G XP_005274096.1:n.-577A>G
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