Canonical Allele Identifier: CA1977295370
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1858688999

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392312del , CM000673.2:g.61392312del GRCh38
NC_000011.9:g.61159784del , CM000673.1:g.61159784del GRCh37
NC_000011.8:g.60916360del NCBI36
NG_032976.1:g.4953del

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-320del ENSP00000440638.1:n.-320del
XM_005274039.3:c.-651del XP_005274096.1:n.-651del
XM_005274039.4:c.-651del XP_005274096.1:n.-651del