Canonical Allele Identifier: CA1977295350
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392287T= , CM000673.2:g.61392287T= GRCh38
NC_000011.9:g.61159759T= , CM000673.1:g.61159759T= GRCh37
NC_000011.8:g.60916335T= NCBI36
NG_032976.1:g.4928T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-345T= ENSP00000440638.1:n.-345T=
XM_005274039.3:c.-676T= XP_005274096.1:n.-676T=
XM_005274039.4:c.-676T= XP_005274096.1:n.-676T=