Canonical Allele Identifier: CA1977295396
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392336C= , CM000673.2:g.61392336C= GRCh38
NC_000011.9:g.61159808C= , CM000673.1:g.61159808C= GRCh37
NC_000011.8:g.60916384C= NCBI36
NG_032976.1:g.4977C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-296C= ENSP00000440638.1:n.-296C=
XM_005274039.3:c.-627C= XP_005274096.1:n.-627C=
XM_005274039.4:c.-627C= XP_005274096.1:n.-627C=