Canonical Allele Identifier: CA2580650764

Gene: TMEM216

Linked Data

• dbSNP Id: rs2135188578
• gnomAD v3: 11-61392331-A-G
• gnomAD v4: 11-61392331-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392331A>G , CM000673.2:g.61392331A>G	GRCh38
NC_000011.9:g.61159803A>G , CM000673.1:g.61159803A>G	GRCh37
NC_000011.8:g.60916379A>G	NCBI36
NG_032976.1:g.4972A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-301A>G	ENSP00000440638.1:n.-301A>G
XM_005274039.3:c.-632A>G	XP_005274096.1:n.-632A>G
XM_005274039.4:c.-632A>G	XP_005274096.1:n.-632A>G