Canonical Allele Identifier: CA2613835795

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392270-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392270T>C , CM000673.2:g.61392270T>C	GRCh38
NC_000011.9:g.61159742T>C , CM000673.1:g.61159742T>C	GRCh37
NC_000011.8:g.60916318T>C	NCBI36
NG_032976.1:g.4911T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-362T>C	ENSP00000440638.1:n.-362T>C
XM_005274039.3:c.-693T>C	XP_005274096.1:n.-693T>C
XM_005274039.4:c.-693T>C	XP_005274096.1:n.-693T>C