Canonical Allele Identifier: CA1977295405
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392344A= , CM000673.2:g.61392344A= GRCh38
NC_000011.9:g.61159816A= , CM000673.1:g.61159816A= GRCh37
NC_000011.8:g.60916392A= NCBI36
NG_032976.1:g.4985A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-288A= ENSP00000440638.1:n.-288A=
XM_005274039.3:c.-619A= XP_005274096.1:n.-619A=
XM_005274039.4:c.-619A= XP_005274096.1:n.-619A=