Canonical Allele Identifier: CA1977295378
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392319A= , CM000673.2:g.61392319A= GRCh38
NC_000011.9:g.61159791A= , CM000673.1:g.61159791A= GRCh37
NC_000011.8:g.60916367A= NCBI36
NG_032976.1:g.4960A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-313A= ENSP00000440638.1:n.-313A=
XM_005274039.3:c.-644A= XP_005274096.1:n.-644A=
XM_005274039.4:c.-644A= XP_005274096.1:n.-644A=