Canonical Allele Identifier: CA678971519

Gene: TMEM216

Linked Data

• dbSNP Id: rs1470927279
• gnomAD v3: 11-61392339-G-C
• gnomAD v4: 11-61392339-G-C
• MyVariant Identifiers: chr11:g.61159811G>C (hg19) ; chr11:g.61392339G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392339G>C , CM000673.2:g.61392339G>C	GRCh38
NC_000011.9:g.61159811G>C , CM000673.1:g.61159811G>C	GRCh37
NC_000011.8:g.60916387G>C	NCBI36
NG_032976.1:g.4980G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-293G>C	ENSP00000440638.1:n.-293G>C
XM_005274039.3:c.-624G>C	XP_005274096.1:n.-624G>C
XM_005274039.4:c.-624G>C	XP_005274096.1:n.-624G>C