Canonical Allele Identifier: CA2613835802

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392277-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392277T>C , CM000673.2:g.61392277T>C	GRCh38
NC_000011.9:g.61159749T>C , CM000673.1:g.61159749T>C	GRCh37
NC_000011.8:g.60916325T>C	NCBI36
NG_032976.1:g.4918T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-355T>C	ENSP00000440638.1:n.-355T>C
XM_005274039.3:c.-686T>C	XP_005274096.1:n.-686T>C
XM_005274039.4:c.-686T>C	XP_005274096.1:n.-686T>C