Canonical Allele Identifier: CA2792319985
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392275C>T , CM000673.2:g.61392275C>T GRCh38
NC_000011.9:g.61159747C>T , CM000673.1:g.61159747C>T GRCh37
NC_000011.8:g.60916323C>T NCBI36
NG_032976.1:g.4916C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-357C>T ENSP00000440638.1:n.-357C>T
XM_005274039.3:c.-688C>T XP_005274096.1:n.-688C>T
XM_005274039.4:c.-688C>T XP_005274096.1:n.-688C>T