Canonical Allele Identifier: CA2792320003
Gene: TMEM216 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392333C>T , CM000673.2:g.61392333C>T GRCh38
NC_000011.9:g.61159805C>T , CM000673.1:g.61159805C>T GRCh37
NC_000011.8:g.60916381C>T NCBI36
NG_032976.1:g.4974C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-299C>T ENSP00000440638.1:n.-299C>T
XM_005274039.3:c.-630C>T XP_005274096.1:n.-630C>T
XM_005274039.4:c.-630C>T XP_005274096.1:n.-630C>T
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