Canonical Allele Identifier: CA2613835847

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392322-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392322T>C , CM000673.2:g.61392322T>C	GRCh38
NC_000011.9:g.61159794T>C , CM000673.1:g.61159794T>C	GRCh37
NC_000011.8:g.60916370T>C	NCBI36
NG_032976.1:g.4963T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-310T>C	ENSP00000440638.1:n.-310T>C
XM_005274039.3:c.-641T>C	XP_005274096.1:n.-641T>C
XM_005274039.4:c.-641T>C	XP_005274096.1:n.-641T>C