Canonical Allele Identifier: CA2613835840
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392317-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392317G>A , CM000673.2:g.61392317G>A GRCh38
NC_000011.9:g.61159789G>A , CM000673.1:g.61159789G>A GRCh37
NC_000011.8:g.60916365G>A NCBI36
NG_032976.1:g.4958G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-315G>A ENSP00000440638.1:n.-315G>A
XM_005274039.3:c.-646G>A XP_005274096.1:n.-646G>A
XM_005274039.4:c.-646G>A XP_005274096.1:n.-646G>A
Search 100 bp 5'
Search 100 bp 3'