Canonical Allele Identifier: CA222894073
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs750063800
MyVariant Identifiers: chr11:g.61159804T>G (hg19) chr11:g.61392332T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392332T>G , CM000673.2:g.61392332T>G GRCh38
NC_000011.9:g.61159804T>G , CM000673.1:g.61159804T>G GRCh37
NC_000011.8:g.60916380T>G NCBI36
NG_032976.1:g.4973T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-300T>G ENSP00000440638.1:n.-300T>G
XM_005274039.3:c.-631T>G XP_005274096.1:n.-631T>G
XM_005274039.4:c.-631T>G XP_005274096.1:n.-631T>G
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