Canonical Allele Identifier: CA599502938

Gene: TMEM216

Linked Data

• dbSNP Id: rs1244936162
• gnomAD v2: 11-61159802-A-G
• gnomAD v3: 11-61392330-A-G
• gnomAD v4: 11-61392330-A-G
• MyVariant Identifiers: chr11:g.61159802A>G (hg19) ; chr11:g.61392330A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392330A>G , CM000673.2:g.61392330A>G	GRCh38
NC_000011.9:g.61159802A>G , CM000673.1:g.61159802A>G	GRCh37
NC_000011.8:g.60916378A>G	NCBI36
NG_032976.1:g.4971A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-302A>G	ENSP00000440638.1:n.-302A>G
XM_005274039.3:c.-633A>G	XP_005274096.1:n.-633A>G
XM_005274039.4:c.-633A>G	XP_005274096.1:n.-633A>G