Canonical Allele Identifier: CA1977295376
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392317G= , CM000673.2:g.61392317G= GRCh38
NC_000011.9:g.61159789G= , CM000673.1:g.61159789G= GRCh37
NC_000011.8:g.60916365G= NCBI36
NG_032976.1:g.4958G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-315G= ENSP00000440638.1:n.-315G=
XM_005274039.3:c.-646G= XP_005274096.1:n.-646G=
XM_005274039.4:c.-646G= XP_005274096.1:n.-646G=