Canonical Allele Identifier: CA1977295348
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392286C= , CM000673.2:g.61392286C= GRCh38
NC_000011.9:g.61159758C= , CM000673.1:g.61159758C= GRCh37
NC_000011.8:g.60916334C= NCBI36
NG_032976.1:g.4927C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-346C= ENSP00000440638.1:n.-346C=
XM_005274039.3:c.-677C= XP_005274096.1:n.-677C=
XM_005274039.4:c.-677C= XP_005274096.1:n.-677C=