Canonical Allele Identifier: CA2792319984
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392274A>G , CM000673.2:g.61392274A>G GRCh38
NC_000011.9:g.61159746A>G , CM000673.1:g.61159746A>G GRCh37
NC_000011.8:g.60916322A>G NCBI36
NG_032976.1:g.4915A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-358A>G ENSP00000440638.1:n.-358A>G
XM_005274039.3:c.-689A>G XP_005274096.1:n.-689A>G
XM_005274039.4:c.-689A>G XP_005274096.1:n.-689A>G