Canonical Allele Identifier: CA2613835830
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392311-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392311G>A , CM000673.2:g.61392311G>A GRCh38
NC_000011.9:g.61159783G>A , CM000673.1:g.61159783G>A GRCh37
NC_000011.8:g.60916359G>A NCBI36
NG_032976.1:g.4952G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-321G>A ENSP00000440638.1:n.-321G>A
XM_005274039.3:c.-652G>A XP_005274096.1:n.-652G>A
XM_005274039.4:c.-652G>A XP_005274096.1:n.-652G>A
Search 100 bp 5'
Search 100 bp 3'