Canonical Allele Identifier: CA2613835863
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392340T>C , CM000673.2:g.61392340T>C GRCh38
NC_000011.9:g.61159812T>C , CM000673.1:g.61159812T>C GRCh37
NC_000011.8:g.60916388T>C NCBI36
NG_032976.1:g.4981T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-292T>C ENSP00000440638.1:n.-292T>C
XM_005274039.3:c.-623T>C XP_005274096.1:n.-623T>C
XM_005274039.4:c.-623T>C XP_005274096.1:n.-623T>C