Canonical Allele Identifier: CA678971510
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1483491648

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392286C>G , CM000673.2:g.61392286C>G GRCh38
NC_000011.9:g.61159758C>G , CM000673.1:g.61159758C>G GRCh37
NC_000011.8:g.60916334C>G NCBI36
NG_032976.1:g.4927C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-346C>G ENSP00000440638.1:n.-346C>G
XM_005274039.3:c.-677C>G XP_005274096.1:n.-677C>G
XM_005274039.4:c.-677C>G XP_005274096.1:n.-677C>G