Canonical Allele Identifier: CA2792319998
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392323A>G , CM000673.2:g.61392323A>G GRCh38
NC_000011.9:g.61159795A>G , CM000673.1:g.61159795A>G GRCh37
NC_000011.8:g.60916371A>G NCBI36
NG_032976.1:g.4964A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-309A>G ENSP00000440638.1:n.-309A>G
XM_005274039.3:c.-640A>G XP_005274096.1:n.-640A>G
XM_005274039.4:c.-640A>G XP_005274096.1:n.-640A>G