Canonical Allele Identifier: CA2613835844
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392321-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392321C>G , CM000673.2:g.61392321C>G GRCh38
NC_000011.9:g.61159793C>G , CM000673.1:g.61159793C>G GRCh37
NC_000011.8:g.60916369C>G NCBI36
NG_032976.1:g.4962C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-311C>G ENSP00000440638.1:n.-311C>G
XM_005274039.3:c.-642C>G XP_005274096.1:n.-642C>G
XM_005274039.4:c.-642C>G XP_005274096.1:n.-642C>G
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