Canonical Allele Identifier: CA938603992

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858690209
• gnomAD v3: 11-61392346-T-C
• gnomAD v4: 11-61392346-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392346T>C , CM000673.2:g.61392346T>C	GRCh38
NC_000011.9:g.61159818T>C , CM000673.1:g.61159818T>C	GRCh37
NC_000011.8:g.60916394T>C	NCBI36
NG_032976.1:g.4987T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-286T>C	ENSP00000440638.1:n.-286T>C
XM_005274039.3:c.-617T>C	XP_005274096.1:n.-617T>C
XM_005274039.4:c.-617T>C	XP_005274096.1:n.-617T>C