Canonical Allele Identifier: CA1977295377

Gene: TMEM216

Linked Data

• dbSNP Id: rs1751326903
• gnomAD v4: 11-61392317-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392317G>C , CM000673.2:g.61392317G>C	GRCh38
NC_000011.9:g.61159789G>C , CM000673.1:g.61159789G>C	GRCh37
NC_000011.8:g.60916365G>C	NCBI36
NG_032976.1:g.4958G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-315G>C	ENSP00000440638.1:n.-315G>C
XM_005274039.3:c.-646G>C	XP_005274096.1:n.-646G>C
XM_005274039.4:c.-646G>C	XP_005274096.1:n.-646G>C