Canonical Allele Identifier: CA2613835834
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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