Canonical Allele Identifier: CA2792319988
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392282T>G , CM000673.2:g.61392282T>G GRCh38
NC_000011.9:g.61159754T>G , CM000673.1:g.61159754T>G GRCh37
NC_000011.8:g.60916330T>G NCBI36
NG_032976.1:g.4923T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-350T>G ENSP00000440638.1:n.-350T>G
XM_005274039.3:c.-681T>G XP_005274096.1:n.-681T>G
XM_005274039.4:c.-681T>G XP_005274096.1:n.-681T>G