Canonical Allele Identifier: CA678971516

Gene: TMEM216

Linked Data

• dbSNP Id: rs1051402574
• gnomAD v3: 11-61392335-C-G
• gnomAD v4: 11-61392335-C-G
• MyVariant Identifiers: chr11:g.61159807C>G (hg19) ; chr11:g.61392335C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392335C>G , CM000673.2:g.61392335C>G	GRCh38
NC_000011.9:g.61159807C>G , CM000673.1:g.61159807C>G	GRCh37
NC_000011.8:g.60916383C>G	NCBI36
NG_032976.1:g.4976C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-297C>G	ENSP00000440638.1:n.-297C>G
XM_005274039.3:c.-628C>G	XP_005274096.1:n.-628C>G
XM_005274039.4:c.-628C>G	XP_005274096.1:n.-628C>G